# U-systems Inc – FDA Inspection, Oct 30, 2008

Source: https://www.keypedia.com/records/fda_inspections/u-systems-inc/5217673a-5d1f-4e03-9113-4325cb8f8c4d
Source feed: FDA_Inspections

> FDA inspection 546257 of U-systems Inc, October 30, 2008. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 546257
- Company Name: U-systems Inc
- Inspection Date: 2008-10-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1006662 - 2017-03-31
- [FDA Inspection 849549 - 2013-09-10](https://www.keypedia.com/records/fda_inspections/u-systems-inc/50c67c18-1822-4318-9930-91dc43937412)
- [FDA Inspection 766597 - 2012-01-26](https://www.keypedia.com/records/fda_inspections/u-systems-inc/b9bfb018-16f6-4558-97db-bd629135810d)

Company: https://www.keypedia.com/companies/u-systems-inc/ece80e1d-895e-4cef-ad7d-54cbf0f5d749

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