# FDA Inspection 1053027 - Cryopen, LLC - March 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/cryopen-llc/8d93b9c1-b45e-470c-96e6-10b301bd0d80
Source feed: FDA_Inspections

> FDA Inspection 1053027 for Cryopen, LLC on March 13, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053027
- Company Name: Cryopen, LLC
- Inspection Date: 2018-03-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 661679 - 2010-04-30](https://www.globalkeysolutions.net/records/fda_inspections/cryopen-llc/3247c9e9-0d67-4d7e-bcc8-5ac2964b23d6)
- [FDA Inspection 661679 - 2010-04-30](https://www.globalkeysolutions.net/records/fda_inspections/cryopen-llc/fa633085-6241-47c9-b3f2-5c8c813b6e28)

Company: https://www.globalkeysolutions.net/companies/cryopen-llc/10c14783-0c13-46df-8afd-6fd8a72656f4

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