# FDA Inspection 666798 - Unotech Diagnostics, Inc. - June 16, 2010

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

> FDA Inspection 666798 for Unotech Diagnostics, Inc. on June 16, 2010. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 666798 - 2010-06-16](https://www.globalkeysolutions.net/api/records/fda_inspections/unotech-diagnostics-inc/138e1b07-973c-4755-a9e4-0516a00b1462/)
- [FDA Inspection 549871 - 2008-12-05](https://www.globalkeysolutions.net/api/records/fda_inspections/unotech-diagnostics-inc/54d97257-aee9-4f27-a246-a285bbe0a0f2/)

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

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