FDA Inspection 821065 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 1421377

The FDA completed an inspection of AndersonBrecon Inc. on March 1, 2013 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
March 1, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)