FDA Inspection 1178267 — Aurolife Pharma LLC

Aurolife Pharma LLC — FEI 3014028588

The FDA completed an inspection of Aurolife Pharma LLC on Aug 26, 2022 in Durham, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Durham, NC (United States)