FDA Inspection 1193412 — Nephron Pharmaceuticals

Nephron Pharmaceuticals — FEI 3010247115

The FDA completed an inspection of Nephron Pharmaceuticals on Dec 2, 2022 in Murray, KY. 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
Dec 2, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Murray, KY (United States)