FDA Inspection 612435 — Ranbaxy Inc.

Ranbaxy Inc. — FEI 3003476632

The FDA completed an inspection of Ranbaxy Inc. on Sep 29, 2009 in Princeton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 29, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Princeton, NJ (United States)

Additional details

Postmarket Adverse Drug Experience (PADE)

Citations

IDCFRDescription
202721 CFR 211.192Investigations of discrepancies, failures

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