FDA Inspection
Bisico Bielefelder Dentalsilicone GmbH & Co. KGBisico Bielefelder Dentalsilicone GmbH & Co. KG – FDA Inspection, Aug 26, 2010
Record Details
This FDA Inspection record concerns Bisico Bielefelder Dentalsilicone GmbH & Co. KG, with an inspection on August 26, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 26, 2010
- Product Type
- Devices
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ID · e2051651-de7e-45e9-bdb9-68a7c8773436
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 684930
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.150Lack of or inadequate procedures for storage.
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Bisico Bielefelder Dentalsilicone GmbH & Co. KG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 20, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bisico Bielefelder Dentalsilicone GmbH & Co. KG
- FDA Inspection 838938 - 2013-06-20
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