# FDA Inspection 939180 - AMCOR Flexibles, Inc. - August 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/amcor-flexibles-inc/84c2bb09-eb9b-4873-b045-cbe0c1fd9e30
Source feed: FDA_Inspections

> FDA Inspection 939180 for AMCOR Flexibles, Inc. on August 17, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 939180
- Company Name: AMCOR Flexibles, Inc.
- Inspection Date: 2015-08-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 725201 - 2011-05-09](https://www.keypedia.com/records/fda_inspections/amcor-flexibles-inc/68101dd9-187f-4dfc-9ab5-c03341f26ef7)

Company: https://www.keypedia.com/companies/amcor-flexibles-inc/d1572287-205b-4e10-a624-debbb7dae90a

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