FDA Inspection 1255484 — Azurity Pharmaceuticals, Inc.

Azurity Pharmaceuticals, Inc. — FEI 3029797518

The FDA completed an inspection of Azurity Pharmaceuticals, Inc. on Nov 14, 2024 in Atlanta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 14, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.