FDA Inspection 738657 — Renaissance Lakewood, LLC

Renaissance Lakewood, LLC — FEI 2242829

The FDA completed an inspection of Renaissance Lakewood, LLC on August 10, 2011 in Lakewood, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 10, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lakewood, NJ (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
189021 CFR 211.165(e)Test methods
358521 CFR 211.110(a)Control procedures to monitor and validate performance