FDA Inspection 662685 — Stillman Co., Inc.

Stillman Co., Inc. — FEI 1410797

The FDA completed an inspection of Stillman Co., Inc. on May 20, 2010 in Aurora, 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
May 20, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Aurora, IL (United States)