FDA Inspection 970690 — Azurity Pharmaceuticals, Inc.

Azurity Pharmaceuticals, Inc. — FEI 3003395329

The FDA completed an inspection of Azurity Pharmaceuticals, Inc. on April 19, 2016 in Woburn, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Woburn, MA (United States)