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FDA Inspection
•BeeAlive, Inc.•January 25, 2012

BeeAlive, Inc. – FDA Inspection, Jan 25, 2012

Record Details

This FDA Inspection record concerns BeeAlive, Inc., with an inspection on January 25, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
BeeAlive, Inc.
Inspection Date
January 25, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 58cf9a91-d6df-454d-a96f-ad0291301e4c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
763990
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

6
  1. 21 CFR 211.56(a)Sanitation--buildings not clean, free of infestation
  2. 21 CFR 211.192Quality control unit review of records
  3. 21 CFR 211.142(a)Quarantine - actual practice
  4. 21 CFR 211.67(c)Cleaning/maintenance records not kept
  5. 21 CFR 211.100(a)Approval and review of procedures
  6. 21 CFR 211.198(a)Complaints reviewed by Quality Control Unit

Full citation text and observation details available on the Dashboard.

Other FDA inspections of BeeAlive, Inc.

4
DateClassificationOfficeProject area
January 18, 2023VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
March 15, 2019VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
March 3, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 1, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for BeeAlive, Inc.
  • FDA Inspection 1196645 - 2023-01-18
  • FDA Inspection 1083128 - 2019-03-15
  • FDA Inspection 712342 - 2011-03-03
  • FDA Inspection 655136 - 2010-04-01

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