FDA Inspection
Kinamed IncKinamed Inc – FDA Inspection, Jun 1, 2010
Record Details
This FDA Inspection record concerns Kinamed Inc, with an inspection on June 1, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kinamed Inc
- Inspection Date
- June 1, 2010
- Product Type
- Devices
View Company Profile
ID · 97761693-6e24-48ef-84dd-fcef723b9e20
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663654
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(c)Investigation of device failures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Kinamed Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 14, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 15, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 27, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kinamed Inc
- FDA Inspection 1117751 - 2020-02-12
- FDA Inspection 980471 - 2016-07-21
- FDA Inspection 875744 - 2014-04-14
- FDA Inspection 773213 - 2012-03-15
- FDA Inspection 609809 - 2009-08-27
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