# FDA Inspection 1248312 - General Meditech Inc - August 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 for General Meditech Inc on August 22, 2024. Classification: Voluntary Action Indicated (VAI).

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

## Related Documents

- [FDA Inspection 1248312 - 2024-08-22](https://www.keypedia.com/records/fda_inspections/general-meditech-inc/3e903cd0-ff7c-4455-a9be-4654368e1fe0)

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