FDA Inspection 983024 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 3003015528

The FDA completed an inspection of AndersonBrecon Inc. on Jul 19, 2016 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
Jul 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)

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