# FDA Inspection 991419 - CytoTherm L.P. - October 27, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/f4a52aa2-64f1-42d5-bc82-6cf66adbf900
Source feed: FDA_Inspections

> FDA Inspection 991419 for CytoTherm L.P. on October 27, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 991419
- Company Name: CytoTherm L.P.
- Inspection Date: 2016-10-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1123811 - 2019-11-14](https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/929f2d54-f0d6-4116-9ca3-be73d6d0dc5e)
- [FDA Inspection 991419 - 2016-10-27](https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/9174ac66-8a7c-4eca-a592-1ccf7d8446f0)
- [FDA Inspection 873309 - 2014-03-31](https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/de62b709-4421-4ee5-80b8-fed0c0923294)
- [FDA Inspection 873309 - 2014-03-31](https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/ac382990-ff1f-4751-b527-b36661ad249c)
- [FDA Inspection 713076 - 2011-03-09](https://www.globalkeysolutions.net/records/fda_inspections/cytotherm-lp/8d311d5a-e2b0-44ff-98c5-75c1346f67f4)

Company: https://www.globalkeysolutions.net/companies/cytotherm-lp/e15a9500-4b13-4cfc-9c38-616a8a7950fe

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7