FDA Inspection
Amcor Flexibles, LLC.Amcor Flexibles, LLC. – FDA Inspection, Sep 14, 2017
Record Details
This FDA Inspection record concerns Amcor Flexibles, LLC., with an inspection on September 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ed0f5a90-d387-4fc0-833b-a218f6d3820a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1025286
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(b)Documentation
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Other FDA inspections of Amcor Flexibles, LLC.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 26, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 2, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Amcor Flexibles, LLC.
- FDA Inspection 1179530 - 2022-08-26
- FDA Inspection 832094 - 2013-05-02
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