# Tytek Medical Inc – FDA Inspection, Jun 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/tytek-medical-inc/896b454f-b41f-4386-be3a-44b59e3cf1dd
Source feed: FDA_Inspections

> FDA inspection 1210081 of Tytek Medical Inc, June 21, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 806. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 4

## Related Documents

- FDA Inspection 1054584 - 2018-04-23

## Related Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

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

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