FDA Inspection 807245 — Ameridose, LLC

Ameridose, LLC — FEI 3005881167

The FDA completed an inspection of Ameridose, LLC on November 9, 2012 in Westborough, MA. 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 9, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Westborough, MA (United States)