FDA Inspection 778570 — Herrin Drug

Herrin Drug — FEI 3004068505

The FDA completed an inspection of Herrin Drug on Apr 26, 2012 in Herrin, IL. 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
Apr 26, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Herrin, IL (United States)