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FDA Inspection
•Vitalab Company, Inc•February 5, 2018

Vitalab Company, Inc – FDA Inspection, Feb 5, 2018

Record Details

This FDA Inspection record concerns Vitalab Company, Inc, with an inspection on February 5, 2018, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Vitalab Company, Inc
Inspection Date
February 5, 2018
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
People
  • Heath W. Cartwright (Company Rep)
  • Kristi B. Panzer (Issuing Officer)
View Company Profile

ID · dd60144a-e140-45b0-acc0-7db9bc512c23

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1039825
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards
Outcome
Form 483 issued

FDA Citations

6
  1. 21 CFR 111.153Written procedures - packaging
  2. 21 CFR 111.205(b)(1)Master manufacturing record - specifications; quality
  3. 21 CFR 111.260(l)(3)Batch record - approved, released, rejected; batch
  4. 21 CFR 111.353Manufacturing operations - written procedures
  5. 21 CFR 111.55Production, process controls - implement
  6. 21 CFR 111.75(f)(1)Containers closures visual ID review suppliers documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Vitalab Company, Inc

7
DateClassificationOfficeProject area
April 19, 2023NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
December 12, 2019NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 14, 2018VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
June 17, 2015NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
May 15, 2014OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 7 other inspections on the company page
Other documents for Vitalab Company, Inc
  • FDA Inspection 1203378 - 2023-04-19
  • FDA Inspection 1116143 - 2019-12-12
  • FDA Inspection 1070524 - 2018-09-14
  • FDA Inspection 930453 - 2015-06-17
  • FDA Inspection 879745 - 2014-05-15

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