# FDA Inspection 1068354 - Genprime Inc - September 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/genprime-inc/3df4a52b-2042-4530-a23c-c39ce7cf3d20
Source feed: FDA_Inspections

> FDA Inspection 1068354 for Genprime Inc on September 13, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1068354
- Company Name: Genprime Inc
- Inspection Date: 2018-09-13
- 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 1068354 - 2018-09-13](https://www.globalkeysolutions.net/records/fda_inspections/genprime-inc/5671e335-35ad-48bb-880e-5b593608e1da)

Company: https://www.globalkeysolutions.net/companies/genprime-inc/d722549c-d1df-4ff0-9a6f-0656a70ff76b

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