FDA Inspection 748939 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 3003015528

The FDA completed an inspection of AndersonBrecon Inc. on October 7, 2011 in Rockford, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 7, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)