# Bisico Bielefelder Dentalsilicone GmbH & Co. KG – FDA Inspection, Aug 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 of Bisico Bielefelder Dentalsilicone GmbH & Co. KG, August 26, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 838938 - 2013-06-20

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