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 Jul 12, 2012 in Iowa City, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 12, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Iowa City, IA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.