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FDA Inspection
•Central Boeki U.S.A. LTD.•July 13, 2023

Central Boeki U.S.A. LTD. – FDA Inspection, Jul 13, 2023

Record Details

This FDA Inspection record concerns Central Boeki U.S.A. LTD., with an inspection on July 13, 2023, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Central Boeki U.S.A. LTD.
Inspection Date
July 13, 2023
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
Person
  • Melissa N. Gregorio (Investigator)
View Company Profile

ID · 0d787dba-7cb6-471d-b9b6-502e9bdf63b6

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1210451
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards
Outcome
Form 483 issued

FDA Citations

12
  1. 21 CFR 123.10HACCP training or qualification
  2. 21 CFR 123.11(b)Sanitation monitoring
  3. 21 CFR 117.35(c)Pest control
  4. 21 CFR 117.93Storage and Distribution
  5. 21 CFR 123.6(b)No HACCP plan
  6. 21 CFR 123.12(a)(2)Importer verification
  7. 21 CFR 117.35(c)Pest control
  8. 21 CFR 117.93Storage and Distribution
  9. 21 CFR 123.10HACCP training or qualification
  10. 21 CFR 123.11(b)Sanitation monitoring

Showing 10 of 12 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Central Boeki U.S.A. LTD.

7
DateClassificationOfficeProject area
October 11, 2024VAINew York District OfficeFoodborne Biological Hazards
January 9, 2020NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
December 11, 2017VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
January 31, 2017OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
December 28, 2012OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 7 other inspections on the company page
Other documents for Central Boeki U.S.A. LTD.
  • FDA Inspection 1251747 - 2024-10-11
  • FDA Inspection 1115243 - 2020-01-09
  • FDA Inspection 1034719 - 2017-12-11
  • FDA Inspection 998363 - 2017-01-31
  • FDA Inspection 812069 - 2012-12-28

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