FDA Inspection 814797 — The Procter & Gamble Co.

The Procter & Gamble Co. — FEI 1523399

The FDA completed an inspection of The Procter & Gamble Co. on November 26, 2012 in Cincinnati, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 26, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Cincinnati, OH (United States)

Citations

IDCFRDescription
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate