FDA Inspection
Biomedical Devices of Kansas, LLCBiomedical Devices of Kansas, LLC – FDA Inspection, Sep 3, 2009
Record Details
This FDA Inspection record concerns Biomedical Devices of Kansas, LLC, with an inspection on September 3, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 3, 2009
- Product Type
- Devices
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ID · 4103af88-98f4-4799-b66e-259e99796381
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 609835
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.22Quality audits - auditor independence
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Other FDA inspections of Biomedical Devices of Kansas, LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 12, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 7, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 5, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Biomedical Devices of Kansas, LLC
- FDA Inspection 1074976 - 2018-12-12
- FDA Inspection 995052 - 2016-12-07
- FDA Inspection 824825 - 2013-03-05
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