# FDA Inspection 1033871 - TDM Surgitech, Inc. - November 28, 2017

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

> FDA Inspection 1033871 for TDM Surgitech, Inc. on November 28, 2017. Classification: Voluntary Action Indicated (VAI).

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

## Related Documents

- [FDA Inspection 1033871 - 2017-11-28](https://www.globalkeysolutions.net/records/fda_inspections/tdm-surgitech-inc/7a01e90f-ebc0-4e5a-99ee-738c43107745)

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

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