FDA Inspection 1151115 — Amcor Flexibles Inc

Amcor Flexibles Inc — FEI 3003243311

The FDA completed an inspection of Amcor Flexibles Inc on September 1, 2021 in Mundelein, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Mundelein, IL (United States)