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U.S. Department of Health and Human Services

Inspections, Compliance, Enforcement, and Criminal Investigations

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Cold Cut Kruise, Inc.

  

Department of Health and Human Services logoDepartment of Health and Human Services

Public Health Service
Food and Drug Administration
 Detroit District
300 River Place
Suite 5900
Detroit, MI 48207
Telephone: 313-393-8100
FAX: 313-393-8139


WARNING LETTER

2010-DET-01


October 15, 2009


VIA FEDERAL EXPRESS


Leo D. LaRose, President
Cold Cut Kruise, Inc.
39916 Jason Court
Novi, Michigan 48375
 

Dear Mr. LaRose:

We inspected your seafood processing facility, located at 39916 Jason Court, Novi, Michigan on
June 23 - July 8, 2009. We found that you have serious violations of the seafood Hazard
Analysis and Critical Control Point (HACCP) regulation, Title 21, Code of Federal Regulations,
Part 123, and the Current Good Manufacturing Practice regulation for foods, Title 21, Code of
Federal Regulations, Part 110 (21 CFR 123 & 110). In accordance with 21 CFR 123.6(g),
failure of a processor of fish or fishery products to have and implement a HACCP plan that
complies with this section or otherwise operate in accordance with the requirements of Part 123,
renders the fish or fishery products adulterated within the meaning of Section 402(a)(4) of the
Federal Food, Drug, and Cosmetic Act (the Act), 21 U.S.C. § 342(a)(4). Accordingly, your tuna
salad and tuna salad sandwiches are adulterated, in that they have been prepared, packed, or held under insanitary conditions whereby they may have been rendered injurious to health. You may find the Act, the seafood HACCP regulation and the Fish and Fisheries Products Hazards & Controls Guidance through links in FDA's home page at www.fda.gov.
 

Your significant violations were as follows:
 

1. You must conduct or have conducted for you a hazard analysis for each kind of fish and
fishery product that you produce to determine whether there are food safety hazards that are reasonably likely to occur and you must have and implement a written HACCP plan to control any food safety hazards that are reasonably likely to occur, to comply with 21 CFR 123.6(a) and (b). However, your fim1 does not have a HACCP plan for tuna salad and tuna salad sandwiches to control the food safety hazards of histamine formation and pathogen growth.
 

For more information concerning the controls for histan1ine formation and pathogen growth,
refer to Chapters 7 and 12, respectively, in the Fish and Fisheries Products Hazards &
Controls Guidance.
 

2. You must maintain sanitation control records that, at a minimum, document monitoring and
corrections set out in 21 CFR 123.11(b), to comply with 21 CFR 123.11(c). However, your
firm did not maintain any sanitation control records for the eight key areas of sanitation that
document sanitation monitoring and correction of sanitation deficiencies for the tuna salad
sandwiches manufactured at your firm.
 

We may take further action if you do not promptly correct these violations. For instance, we may take further action to seize your product(s) and/or enjoin your firm from operating.

You should respond in writing within fifteen (15) working days from your receipt of this letter.
Your response should outline the specific things you are doing to correct these violations. You
should include in your response documentation such as HACCP and verification records, or other
useful information that would assist us in evaluating your corrections. If you cannot complete all
corrections before you respond, you should explain the reason for your delay and state when you
will correct any remaining violations.
 

This letter may not list all the violations at your facility. You are responsible for ensuring that
your processing plant operates in compliance with the Act, the seafood HACCP regulation (2 I
CFR Part 123) and the Current Good Manufacturing Practice regulation (21 CFR Part 110). You
also have a responsibility to use procedures to prevent further violations of the Act and all
applicable regulations.
 

Please send your reply to the Food and Drug Administration, Attention: LCDR Anastasia M.
Piliafas-Brown, Compliance Officer, U.S. Food and Drug Administration, 300 River Place, Suite
5900, Detroit, Michigan, 48207. If you have questions regarding any issues in this letter, please
contact LCDR Piliafas-Brown at (313) 393-8100.
 

Sincerely,

/S/

Joann M. Givens
District Director
Detroit District Office