FDA inspection

Amcor Flexibles, LLC.: FDA inspection ending Sep 14, 2017

FDA inspection 1025286 · Voluntary Action Indicated (VAI) · Commerce, CA

Key facts

Inspection ID 1025286
Firm Amcor Flexibles, LLC.
FEI number 2023811
Address 5416 Union Pacific Ave
City Commerce
State CA
ZIP 90022
Country United States
Fiscal year 2017
Inspection end date Sep 14, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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