FDA Inspection 1151115 — Amcor Flexibles, LLC

Amcor Flexibles, LLC — FEI 3003243311

The FDA completed an inspection of Amcor Flexibles, LLC on Sep 1, 2021 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
Sep 1, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Mundelein, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.