FDA Inspection 571865 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 1421377

The FDA completed an inspection of AndersonBrecon Inc. on Mar 20, 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
Mar 20, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)

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