FDA Inspection 582163 — The Procter & Gamble Co.

The Procter & Gamble Co. — FEI 1523399

The FDA completed an inspection of The Procter & Gamble Co. on April 24, 2009 in Cincinnati, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 24, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Cincinnati, OH (United States)