FDA Inspection 1163069 — AndersonBrecon Inc.

AndersonBrecon Inc. — FEI 3003015528

The FDA completed an inspection of AndersonBrecon Inc. on February 25, 2022 in Rockford, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 25, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Rockford, IL (United States)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented