# General Meditech Inc – FDA Inspection, Aug 22, 2024

Source: https://www.keypedia.com/records/fda_inspections/general-meditech-inc/5909e583-023d-4cab-b37b-a89c9f34365a
Source feed: FDA_Inspections

> FDA inspection 1248312 of General Meditech Inc, August 22, 2024. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803, 820 and 830. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1248312
- Company Name: General Meditech Inc
- Inspection Date: 2024-08-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1026399 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/general-meditech-inc/1c52155d-e04d-48ee-8635-5c7713e7ae2c)

## Related Officers

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

Company: https://www.keypedia.com/companies/general-meditech-inc/7fbe9344-de29-418e-95a3-23330acea444

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