# FDA Inspection 988942 - Amcor Flexibles Inc - September 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/amcor-flexibles-inc/7f38ee02-2b58-44e4-be21-3226ffbee74e
Source feed: FDA_Inspections

> FDA Inspection 988942 for Amcor Flexibles Inc on September 09, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988942
- Company Name: Amcor Flexibles Inc
- Inspection Date: 2016-09-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1151115 - 2021-09-01](https://www.keypedia.com/records/fda_inspections/amcor-flexibles-inc/2bcfff20-4453-4e42-9436-d9e5e4b295a9)
- [FDA Inspection 1151115 - 2021-09-01](https://www.keypedia.com/records/fda_inspections/amcor-flexibles-inc/0a6bbea7-9cbb-48f6-80d3-d3ee38376946)

Company: https://www.keypedia.com/companies/amcor-flexibles-inc/5c4433be-b48c-4fa7-afa8-ced27c9f9a8e

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