FDA Inspection 671773 — Germiphene Corporation

Germiphene Corporation — FEI 3000166001

The FDA completed an inspection of Germiphene Corporation on Jun 24, 2010 in Brantford. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 24, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Brantford (Canada)

Citations

IDCFRDescription
331221 CFR 820.120(d)Mixups
369021 CFR 820.100(a)(3)Identification of actions needed