# Amcor Flexibles, LLC. – FDA Inspection, Sep 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/amcor-flexibles-llc/ed0f5a90-d387-4fc0-833b-a218f6d3820a
Source feed: FDA_Inspections

> FDA inspection 1025286 of Amcor Flexibles, LLC., September 14, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025286
- Company Name: Amcor Flexibles, LLC.
- Inspection Date: 2017-09-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1179530 - 2022-08-26
- [FDA Inspection 832094 - 2013-05-02](https://www.keypedia.com/records/fda_inspections/amcor-flexibles-llc/d9a112a4-1be7-4e31-bb07-99b3da5323e0)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.keypedia.com/companies/amcor-flexibles-llc/a987255c-32b8-4f02-a1e9-6b2aa50226b0

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7