# Unotech Diagnostics, Inc. – FDA Inspection, Jun 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/unotech-diagnostics-inc/f972d675-064f-42ca-801e-2c305202e89b
Source feed: FDA_Inspections

> FDA inspection 666798 of Unotech Diagnostics, Inc., June 16, 2010. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 666798
- Company Name: Unotech Diagnostics, Inc.
- Inspection Date: 2010-06-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 549871 - 2008-12-05

Company: https://www.keypedia.com/companies/unotech-diagnostics-inc/50726f91-711f-4092-8003-dee96edfa0f2

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