FDA Inspection 1232498 — AltaThera Pharmaceuticals LLC

AltaThera Pharmaceuticals LLC — FEI 3013989010

The FDA completed an inspection of AltaThera Pharmaceuticals LLC on February 23, 2024 in Chicago, IL. 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
February 23, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)