# TDM Surgitech, Inc. – FDA Inspection, Nov 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/tdm-surgitech-inc/af92f216-2921-4af3-a052-497abcb77af3
Source feed: FDA_Inspections

> FDA inspection 1033871 of TDM Surgitech, Inc., November 28, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1033871
- Company Name: TDM Surgitech, Inc.
- Inspection Date: 2017-11-28
- 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: 6

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/tdm-surgitech-inc/60b6aecb-7a02-4ba0-a178-1dee357b12c3

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