# FDA Inspection 1214483 - Surgitech Inc - August 10, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/surgitech-inc/2b32b1d2-ee7e-4855-8c0f-d015fda5b52d
Source feed: FDA_Inspections

> FDA Inspection 1214483 for Surgitech Inc on August 10, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1214483
- Company Name: Surgitech Inc
- Inspection Date: 2023-08-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1214483 - 2023-08-10](https://www.globalkeysolutions.net/records/fda_inspections/surgitech-inc/c90b0e59-a59a-490a-b250-80f76797d701)
- [FDA Inspection 1023579 - 2017-08-23](https://www.globalkeysolutions.net/records/fda_inspections/surgitech-inc/1bc066d5-23d0-4fdb-8336-64af555cd676)
- [FDA Inspection 1023579 - 2017-08-23](https://www.globalkeysolutions.net/records/fda_inspections/surgitech-inc/c6eb683b-f42d-40b7-80a9-e9f213f27879)

Company: https://www.globalkeysolutions.net/companies/surgitech-inc/2272bfc6-a009-4b35-bdac-84f8c10cb783

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