# FDA Inspection 1210081 - Tytek Medical Inc - June 21, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/tytek-medical-inc/08cd1ad0-7ba5-4191-b900-f70cb2eb0578
Source feed: FDA_Inspections

> FDA Inspection 1210081 for Tytek Medical Inc on June 21, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210081
- Company Name: Tytek Medical Inc
- Inspection Date: 2023-06-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1210081 - 2023-06-21](https://www.globalkeysolutions.net/records/fda_inspections/tytek-medical-inc/896b454f-b41f-4386-be3a-44b59e3cf1dd)
- [FDA Inspection 1054584 - 2018-04-23](https://www.globalkeysolutions.net/records/fda_inspections/tytek-medical-inc/77452fa9-3eb3-4392-b4af-e45211d7cd9b)
- [FDA Inspection 1054584 - 2018-04-23](https://www.globalkeysolutions.net/records/fda_inspections/tytek-medical-inc/78bd8c1b-0acc-4c5a-907f-800ff6c6b5ef)

Company: https://www.globalkeysolutions.net/companies/tytek-medical-inc/422cbd57-4e14-4769-a409-abbc74b50520

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