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FDA Inspection 1100331 — Renaissance Lakewood, LLC

Renaissance Lakewood, LLC — FEI 2242829

The FDA completed an inspection of Renaissance Lakewood, LLC on August 22, 2019 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
August 22, 2019
Fiscal Year
2019
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))
  • 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))
  • 911163 (VAI Fri Feb 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources