FDA Inspection 1329448 — Amcor Flexibles, LLC

Amcor Flexibles, LLC — FEI 3003243311

The FDA completed an inspection of Amcor Flexibles, LLC on Jul 28, 2026 in Mundelein, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 28, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Mundelein, IL (United States)