FDA Inspection 763990 — BeeAlive, Inc.

BeeAlive, Inc. — FEI 2435065

The FDA completed an inspection of BeeAlive, Inc. on January 25, 2012 in Congers, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 25, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Congers, NY (United States)

Citations

IDCFRDescription
122721 CFR 211.67(c)Cleaning/maintenance records not kept
177421 CFR 211.142(a)Quarantine - actual practice
202621 CFR 211.192Quality control unit review of records
355921 CFR 211.56(a)Sanitation--buildings not clean, free of infestation
357021 CFR 211.100(a)Approval and review of procedures
438821 CFR 211.198(a)Complaints reviewed by Quality Control Unit