FDA Inspection 652318 — Gemini Pharmaceuticals, Inc.

Gemini Pharmaceuticals, Inc. — FEI 2432926

The FDA completed an inspection of Gemini Pharmaceuticals, Inc. on March 23, 2010 in Commack, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 23, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Commack, NY (United States)

Citations

IDCFRDescription
125621 CFR 211.68(b)Backup file not maintained
126321 CFR 211.68(b)Computer control of master formula records