FDA Inspection 636433 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 1421377

The FDA completed an inspection of AndersonBrecon Inc. on Dec 18, 2009 in Rockford, 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
Dec 18, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)