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Association of Food & Drug Officials
 
 
       June 17, 2008

 

Division of Dockets Management (HFA-305)
Food and Drug Administration
5630 Fishers Lane
, Room 1061
Rockville
, MD 20852

Food Protection Plan; OutreachActivities; Opportunity for Public Comment
Docket No. FDA-2008-N-0188
Comments from the Association of Food & Drug Officials

The Association of Food and Drug Officials (AFDO) is a non-profit professional organization consisting of state, federal, and local regulatory officials as members, with industry representatives participating as associate members. From its very inception over 110 years ago, AFDO has recognized the need for uniform laws and regulations and has actively promoted uniformity and cooperation among regulatory agencies at all levels. AFDO has also promoted theconcept of a fully integrated food safety system for this country, which utilizes the resources, and authorities of all levels of government as an effective means for meeting food safety challenges that exist. FDA’s Food Protection Plan appears to embrace this concept and AFDO is pleased to offer our specific comments to this strategy. We have supplied similar remarks previously but wish to submit the following for the record:

 

1.               There is not much mention in the plan of state and local government agencies, the number of services they provide for the cause,nor how they can and will be utilized as first responders for prevention,assurance and response.

2.               There needs to be more details presented on the specific working relationship that is envisioned between FDA and the states andlocals.  The document addresses the issue, but in very broad and vague terms.

3.               The plan includes three core elements of protection:Prevent, Intervene, and Respond. It could have included a fourth: Educate.  In order to promote increased corporate responsibility, industry must be educated on what we as science basedexperts believe they can do better to avert the threat of new or existing pathogens...especially those facilities in foreign countries.

4.               The Office of Management and Budget (OMB) recently approved the Manufactured Food Regulatory Program Standards that were recently developed by FDA and state food safety officials. These standards represent recognized best practices of a high-quality risk-based regulatory program, and if complied with can demonstrate a states equivalency to FDA. FDA needs to speed up the implementation process for these standards so more states can participate in the assessment of their food safety program. FDA can then share inspection work plans with state agencies to avoid duplication of efforts.

5.               FDA must begin to accept state food laboratory analysis of foods so they can better work with the states on sampling assignments and the sharing of surveillance data. Work performed here should include both imported and domestic products.

6.               FDA must improve their presence in foreign countries.By gaining confidence with state and local governments handling most of the domestic burden, FDA should be able to achieve this goal. A number of states are performing inspection verification for foreign dairy manufacturers of Grade A products. FDA should be performing these inspections.

7.               A number of states are leading the way in mandatory requirements for vegetable growers and packers. California,Florida, and Virginia have all introduced mandatory programs for specific commodities in their states. FDA should model these programs so they become nationally accepted.

8.               There is a huge need to improve our response efforts with food recalls. Recent national recalls for peanut butter, spinach, and chili sauce were too confusing and ineffective. Distribution lists for recalled food products are not readily shared by FDA with state officials and, in many cases, shared very late. As a result, state and local officials must send their field staff out into warehouses and stores searching for these products wherever possible. This is wasteful and very ineffective, but seems to be the only option available to us at this time. North Carolina recently employed an Incident Command System (ICS) utilizing state and local government officials from a multitude of agencies within that state to address the recent chili sauce recall. They performed more recall audit checks in North Carolina than the rest of the country combined. They also found a large number of these botulism-tainted products in children’s camps and other non-traditional food venues ready for sale or service. FDA needs to review their response efforts with recalls and establish a formalized strategy with state and local government to better deal with recalls.

9.               We strongly support FDA developing cooperative agreements with states, local agencies, or their representative organizations that will assist in advancing integrated projects. These agreements can be based on current successful programs, which exist around the country.

10.           The plan does not include recommendations for amendments to the Federal Food, Drug, and Cosmetic Act that would give FDA more power/authority over prevention.  Current law is mainly for enforcement,including reacting to problems rather than preventing problems.

11.           The plan does not provide for, nor advocate strongly enough, for adequate funding for the FDA to be an agency engaged in prevention.  Inspections are considered to be preventive if they are done on schedule and within a reasonable period of time.  In Texas, for instance, inspectors review the previous inspection report and report back on the numbers of “voluntary corrections” a company has made since the previous inspection. More than24,000 “voluntary corrections” at food processors and wholesale distributors occur each year, and which may prevent a significant number of illnesses.

12.           The document needs to call for a budget line item for state contracts/ partnerships/cooperative agreements.  Without this authority we believe initial funding will disappear in a few years.

13.           With the exception of Seafood and Juice HACCP, FDA’s current regulations are all “command and control” regulations.  FDA needs to address all food regulation to permit industry innovation. One potential way to accomplish this is by mandating HACCP principles of all food processors.

AFDO looks forward to working with FDA in any fashion possible to advance the Food Protection Plan, develop a more integrated strategy for addressing food safety issues, and enhance consumer confidence in the safety of our food supply.

   

 
Respectfully submitted,



Gerald Wojtala, President
Association of Food and Drug Officials
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