FDA Inspection
CytoTherm L.P.CytoTherm L.P. – FDA Inspection, Mar 31, 2014
Record Details
This FDA Inspection record concerns CytoTherm L.P., with an inspection on March 31, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- CytoTherm L.P.
- Inspection Date
- March 31, 2014
- Product Type
- Devices
View Company Profile
ID · de62b709-4421-4ee5-80b8-fed0c0923294
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 873309
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of CytoTherm L.P.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 14, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 9, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for CytoTherm L.P.
- FDA Inspection 1123811 - 2019-11-14
- FDA Inspection 991419 - 2016-10-27
- FDA Inspection 713076 - 2011-03-09
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