# FDA Inspection 1066596 - Ajex Meditech Ltd - July 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/ajex-meditech-ltd/2c062bb9-e8e5-4943-93c3-bda736be58c1
Source feed: FDA_Inspections

> FDA Inspection 1066596 for Ajex Meditech Ltd on July 12, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066596
- Company Name: Ajex Meditech Ltd
- Inspection Date: 2018-07-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1066596 - 2018-07-12](https://www.keypedia.com/records/fda_inspections/ajex-meditech-ltd/c7531764-0b9f-4061-ac85-74b37fe5a23f)

Company: https://www.keypedia.com/companies/ajex-meditech-ltd/e09b6dd7-039a-449b-99cc-4c303d15b48f

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