# CytoTherm L.P. – FDA Inspection, Oct 27, 2016

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

> FDA inspection 991419 of CytoTherm L.P., October 27, 2016. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991419
- Company Name: CytoTherm L.P.
- Inspection Date: 2016-10-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1123811 - 2019-11-14](https://www.keypedia.com/records/fda_inspections/cytotherm-lp/929f2d54-f0d6-4116-9ca3-be73d6d0dc5e)
- [FDA Inspection 873309 - 2014-03-31](https://www.keypedia.com/records/fda_inspections/cytotherm-lp/de62b709-4421-4ee5-80b8-fed0c0923294)
- FDA Inspection 713076 - 2011-03-09

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/meredith-l-sheridan/4021bfe4-3d32-44da-8dc2-e85d1807c000)

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

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