FDA Inspection 962166 — Germiphene Corporation

Germiphene Corporation — FEI 3000166001

The FDA completed an inspection of Germiphene Corporation on Feb 19, 2016 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brantford (Canada)