FDA Inspection 1012257 — L'Oreal USA Products Inc

L'Oreal USA Products Inc — FEI 1000122130

The FDA completed an inspection of L'Oreal USA Products Inc on March 31, 2017 in Somerset, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 31, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Somerset, NJ (United States)