# Bemis Manufacturing Co. – FDA Inspection, Oct 4, 2011

Source: https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/4dd83645-f64f-4026-8b0f-170d33f14246
Source feed: FDA_Inspections

> FDA inspection 748330 of Bemis Manufacturing Co., October 04, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- 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: 2

## Related Documents

- FDA Inspection 1269501 - 2025-04-30
- [FDA Inspection 1099553 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/8794a680-2d80-46c9-9fd1-551d15d4148b)

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