# UMA, Inc. – FDA Inspection, May 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/uma-inc/850e5c67-9527-4a35-90df-8f0bf0cc96c0
Source feed: FDA_Inspections

> FDA inspection 1016417 of UMA, Inc., May 31, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016417
- Company Name: UMA, Inc.
- Inspection Date: 2017-05-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- FDA Inspection 1118756 - 2019-11-21
- FDA Inspection 545897 - 2008-11-10

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/joey-c-west/4ecce3be-9f8f-40eb-a7ff-0364f5864bfa)

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