FDA Inspection 1012418 — The Procter & Gamble Company

The Procter & Gamble Company — FEI 3000719926

The FDA completed an inspection of The Procter & Gamble Company on May 10, 2017 in Mason, OH. 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
May 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mason, OH (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)