FDA Inspection 789750 — The Procter & Gamble Manufacturing Company

The Procter & Gamble Manufacturing Company — FEI 1913771

The FDA completed an inspection of The Procter & Gamble Manufacturing Company on July 12, 2012 in Iowa City, IA. 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
July 12, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Iowa City, IA (United States)