# FDA Inspection 1118756 - UMA, Inc. - November 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/uma-inc/d27fa804-b797-42dc-bdf0-864d4233c522
Source feed: FDA_Inspections

> FDA Inspection 1118756 for UMA, Inc. on November 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1118756
- Company Name: UMA, Inc.
- Inspection Date: 2019-11-21
- 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 1118756 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/uma-inc/3a49c54f-81b7-4e72-89ff-4be1705e6bbf)
- [FDA Inspection 1016417 - 2017-05-31](https://www.keypedia.com/records/fda_inspections/uma-inc/850e5c67-9527-4a35-90df-8f0bf0cc96c0)
- [FDA Inspection 545897 - 2008-11-10](https://www.keypedia.com/records/fda_inspections/uma-inc/937e6243-9344-4f5c-a4be-edb3af9f0446)

Company: https://www.keypedia.com/companies/uma-inc/dc9273ca-7df0-4582-8e92-e4241f2f71e0

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