# FDA Inspection 684930 - Bisico Bielefelder Dentalsilicone GmbH & Co. KG - August 26, 2010

Source: https://www.keypedia.com/records/fda_inspections/bisico-bielefelder-dentalsilicone-gmbh-co-kg/e2051651-de7e-45e9-bdb9-68a7c8773436
Source feed: FDA_Inspections

> FDA Inspection 684930 for Bisico Bielefelder Dentalsilicone GmbH & Co. KG on August 26, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 684930
- Company Name: Bisico Bielefelder Dentalsilicone GmbH & Co. KG
- Inspection Date: 2010-08-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838938 - 2013-06-20](https://www.keypedia.com/records/fda_inspections/bisico-bielefelder-dentalsilicone-gmbh-co-kg/232f845e-3320-49cb-b085-29f0c687649e)
- [FDA Inspection 684930 - 2010-08-26](https://www.keypedia.com/records/fda_inspections/bisico-bielefelder-dentalsilicone-gmbh-co-kg/0dac05fc-280c-4f02-996e-6e82fc9fb737)

Company: https://www.keypedia.com/companies/bisico-bielefelder-dentalsilicone-gmbh-co-kg/56ff8e73-dbd0-4239-a383-c36da5d0dc9b

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