# FDA Inspection 1038456 - Diversilabs - December 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/diversilabs/894a5f01-57ad-43dc-90da-764c170ac952
Source feed: FDA_Inspections

> FDA Inspection 1038456 for Diversilabs on December 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038456
- Company Name: Diversilabs
- Inspection Date: 2017-12-21
- 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 1192515 - 2022-11-14](https://www.keypedia.com/records/fda_inspections/diversilabs/e314c2d7-048f-47a1-9e8b-e01960fae103)
- [FDA Inspection 1038456 - 2017-12-21](https://www.keypedia.com/records/fda_inspections/diversilabs/93348d61-0f58-4b19-9d79-bc7d39a8a2f7)

Company: https://www.keypedia.com/companies/diversilabs/bbe39221-37ea-4011-bd19-10ade1f1996f

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