FDA Inspection 777806 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 1421377

The FDA completed an inspection of AndersonBrecon Inc. on April 19, 2012 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
April 19, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)