FDA Inspection 590065 — ANIP Aquisition Company

ANIP Aquisition Company — FEI 3006171780

The FDA completed an inspection of ANIP Aquisition Company on June 19, 2009 in Windsor Mill, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 19, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Windsor Mill, MD (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Citations

IDCFRDescription
673021 CFR 314.80(b)Failure to develop written procedures
673221 CFR 314.80(c)(1)(i)Late submission of 15-day report
683021 CFR 314.80(c)(2)Interval
683121 CFR 314.80(c)(2)Late submission of quarterly safety reports
891221 CFR 314.81(b)(2)Timely submission