# FDA Inspection 1061408 - Prytime Medical Devices, Inc. - July 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/prytime-medical-devices-inc/6aa34962-7dfe-4835-bf95-d27545ef64b3
Source feed: FDA_Inspections

> FDA Inspection 1061408 for Prytime Medical Devices, Inc. on July 17, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061408
- Company Name: Prytime Medical Devices, Inc.
- Inspection Date: 2018-07-17
- 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 1061408 - 2018-07-17](https://www.globalkeysolutions.net/records/fda_inspections/prytime-medical-devices-inc/1dc1b2f2-74ed-44a6-a1e4-938d844c3f5d)

Company: https://www.globalkeysolutions.net/companies/prytime-medical-devices-inc/68ce214a-991a-463e-9e27-8bb111cd9d4c

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