# FDA Inspection 748330 - Bemis Manufacturing Co. - October 04, 2011

Source: https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/4ce1c347-3ef7-49b8-87f3-3b09b8000f95
Source feed: FDA_Inspections

> FDA Inspection 748330 for Bemis Manufacturing Co. on October 04, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 748330
- Company Name: Bemis Manufacturing Co.
- Inspection Date: 2011-10-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/bemis-manufacturing-co/4730d9b9-dc78-4897-ba54-82711a13c477

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