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WARNING LETTER
•Caito Fisheries Inc•September 4, 2012

Caito Fisheries Inc – FDA Warning Letter, Sep 4, 2012

Record Details

The FDA inspected Caito Fisheries, Inc.'s seafood processing facility in San Francisco, CA, from August 22 to September 4, 2012, and found serious violations of the seafood Hazard Analysis and Critical Control Point (HACCP) regulation (21 CFR Part 123). This renders their seafood products, including fresh, refrigerated scombroid finfish Albacore Tuna, fresh, refrigerated raw Dungeness Crab, and refrigerated, ready-to-eat cooked Dungeness Crab, adulterated under Section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act).

The firm's September 25, 2012, response to the FDA 483 was inadequate due to incomplete HACCP plans. Significant violations include: 1. Failure to have a HACCP plan for receiving and storing ready-to-eat cooked Dungeness Crab to control pathogen growth and toxin formation (21 CFR 123.6(a) and (b)). 2. HACCP plans for Albacore Tuna and Dungeness Crab do not list undeclared allergens as a food safety hazard (21 CFR 123.6(a) and (c)(1)). 3. HACCP plans for Dungeness Crab and Fresh Albacore Tuna do not list "Finished Product Storage" as a critical control

Company
Caito Fisheries Inc
Inspection date
September 4, 2012
Product type
Food
Office
Department of Health and Human Services
People
  • Barbara J. Cassens (Director )
  • Lawton W. Lum (Director of Compliance Branch)
  • Juliane Jung-Lau
  • Michael Gutierrez (Astrophysics)
View Company Profile

ID · 708ddafc-3234-4e1b-a54b-f60939b7f083

Violation Codes10
21 CFR 12321 CFR 123.6(g)21 U.S.C. 342(a)(4)21 CFR 123.6(a)21 CFR 123.6(b)21 CFR 123.6(c)21 CFR 123.6(c)(1)21 CFR 123.3(f)21 CFR 123.6(c)(2)21 CFR 123.3(b)

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