FDA Inspection 562710 — Nephron Pharmaceuticals

Nephron Pharmaceuticals — FEI 3004462991

The FDA completed an inspection of Nephron Pharmaceuticals on Nov 4, 2008 in Mountain Home, ID. 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 4, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mountain Home, ID (United States)