# FDA Inspection 707589 - Unity Tool, Inc. - December 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/unity-tool-inc/1a026d67-c5fd-4789-997f-9c2f24467632
Source feed: FDA_Inspections

> FDA Inspection 707589 for Unity Tool, Inc. on December 21, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 707589
- Company Name: Unity Tool, Inc.
- Inspection Date: 2010-12-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1150479 - 2021-07-15](https://www.keypedia.com/records/fda_inspections/unity-tool-inc/40ac97fd-ac34-4737-96c3-deae94b07631)
- [FDA Inspection 937161 - 2015-07-30](https://www.keypedia.com/records/fda_inspections/unity-tool-inc/d28619a6-f7a5-450c-b87f-a31ade7fa75e)

Company: https://www.keypedia.com/companies/unity-tool-inc/a5e26960-3305-4b6c-9db9-5fc53d15be35

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