FDA Inspection 1248325 — Apnar Pharma LP

Apnar Pharma LP — FEI 3023702739

The FDA completed an inspection of Apnar Pharma LP on August 16, 2024 in Chino, CA. 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
August 16, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chino, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)