FDA Inspection 1123811 — CytoTherm L.P.
The FDA completed an inspection of CytoTherm L.P. on November 14, 2019 in Trenton, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 14, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Trenton, NJ (United States)