# FDA Inspection 1099553 - Bemis Manufacturing Co. - August 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/2df40128-aece-4a39-b017-4f50cd41edec
Source feed: FDA_Inspections

> FDA Inspection 1099553 for Bemis Manufacturing Co. on August 14, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099553
- Company Name: Bemis Manufacturing Co.
- Inspection Date: 2019-08-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1269501 - 2025-04-30](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/1a04a1e8-6add-4bf7-affd-dcb56827c802)
- [FDA Inspection 1269501 - 2025-04-30](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/a92b5287-6e01-4821-89af-31a8f13fbd55)
- [FDA Inspection 1269501 - 2025-04-30](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/3333246f-02f4-4f64-9c29-ab562be9137f)
- [FDA Inspection 1099553 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/8794a680-2d80-46c9-9fd1-551d15d4148b)
- [FDA Inspection 748330 - 2011-10-04](https://www.keypedia.com/records/fda_inspections/bemis-manufacturing-co/4dd83645-f64f-4026-8b0f-170d33f14246)

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