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FDA Inspection
•Continental Vitamin Company Inc•October 26, 2017

Continental Vitamin Company Inc – FDA Inspection, Oct 26, 2017

Record Details

This FDA Inspection record concerns Continental Vitamin Company Inc, with an inspection on October 26, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Continental Vitamin Company Inc
Inspection Date
October 26, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Stephanie A. Slater
View Company Profile

ID · 1b82f06f-4f88-4a27-bb4a-a685c330ff15

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1029902
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.68(a)Calibration/Inspection/Checking not done
  2. 21 CFR 211.22(a)Authority lacking to review records, investigate errors
  3. 21 CFR 211.180(e)(2)Items to cover on annual reviews

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Continental Vitamin Company Inc

3
DateClassificationOfficeProject area
March 30, 2022VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
April 30, 2018NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
April 2, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Continental Vitamin Company Inc
  • FDA Inspection 1166241 - 2022-03-30
  • FDA Inspection 1056101 - 2018-04-30
  • FDA Inspection 829858 - 2013-04-02

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