FDA Inspection 953334 — L'Oreal USA Products Inc

L'Oreal USA Products Inc — FEI 2243054

The FDA completed an inspection of L'Oreal USA Products Inc on December 9, 2015 in Piscataway, 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
December 9, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Piscataway, NJ (United States)