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FDA Inspection 911163 — Renaissance Lakewood, LLC

Renaissance Lakewood, LLC — FEI 2242829

The FDA completed an inspection of Renaissance Lakewood, LLC on February 6, 2015 in Lakewood, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 6, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lakewood, NJ (United States)

Facility

Other inspections at this facility

  • 1209603 (VAI Tue Jun 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1100331 (VAI Thu Aug 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1045720 (VAI Thu Mar 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1009890 (NAI Wed Apr 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 973346 (NAI Wed Jun 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources