# FDA Inspection 782301 - Karex Industries Sdn Bhd - April 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/karex-industries-sdn-bhd/675fa68e-e29c-4069-acb7-6e5e4a21b4ae
Source feed: FDA_Inspections

> FDA Inspection 782301 for Karex Industries Sdn Bhd on April 19, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 782301
- Company Name: Karex Industries Sdn Bhd
- Inspection Date: 2012-04-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 782301 - 2012-04-19](https://www.keypedia.com/records/fda_inspections/karex-industries-sdn-bhd/34d6f511-273f-4937-b3f4-8284e9690555)

Company: https://www.keypedia.com/companies/karex-industries-sdn-bhd/8c4ba8e7-1195-4e46-a9f6-d1be8bbed4d3

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