FDA Inspection 1194959 — Amcor Rigid Packaging USA, LLC

Amcor Rigid Packaging USA, LLC — FEI 3004388281

The FDA completed an inspection of Amcor Rigid Packaging USA, LLC on January 12, 2023 in Fort Worth, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 12, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fort Worth, TX (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements