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FDA Inspection
•Catalina Offshore Products, Inc•November 25, 2013

Catalina Offshore Products, Inc – FDA Inspection, Nov 25, 2013

Record Details

This FDA Inspection record concerns Catalina Offshore Products, Inc, with an inspection on November 25, 2013, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Catalina Offshore Products, Inc
Inspection Date
November 25, 2013
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 0c462711-28ae-4752-a0b4-da0323021cff

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
859738
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards

FDA Citations

11
  1. 21 CFR 123.11(c)Sanitation Records
  2. 21 CFR 123.11(b)Sanitation monitoring
  3. 21 CFR 123.6(b)HACCP plan implementation
  4. 21 CFR 123.7(a)Corrective action per predetermined plan
  5. 21 CFR 123.6(b)No HACCP plan
  6. 21 CFR 123.12(a)(2)Importer verification
  7. 21 CFR 123.7(d)Corrective action documentation
  8. 21 CFR 123.6(c)(3)Critical limits
  9. 21 CFR 123.9(a)Records - content
  10. 21 CFR 123.8(a)(3)(i)Monitoring record review adequacy

Showing 10 of 11 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Catalina Offshore Products, Inc

7
DateClassificationOfficeProject area
July 21, 2025NAILos Angeles District OfficeFood Composition, Standards, Labeling, and Economics
March 16, 2022VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
August 9, 2019VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
August 16, 2016NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
September 22, 2014VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 7 other inspections on the company page
Other documents for Catalina Offshore Products, Inc
  • FDA Inspection 1258622 - 2025-07-21
  • FDA Inspection 1164775 - 2022-03-16
  • FDA Inspection 1100087 - 2019-08-09
  • FDA Inspection 981819 - 2016-08-16
  • FDA Inspection 896807 - 2014-09-22

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