FDA Inspection 951835 — Dermazone LLC

Dermazone LLC — FEI 1000113908

The FDA completed an inspection of Dermazone LLC on November 24, 2015 in Saint Petersburg, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 24, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Petersburg, FL (United States)