FDA Inspection 947995 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 1450819

The FDA completed an inspection of AndersonBrecon Inc. on October 16, 2015 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
October 16, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockford, IL (United States)