# FDA Inspection 678543 - DeRoyal Industries Inc - August 26, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/deroyal-industries-inc/dd2a5097-c0bf-4fb4-abbb-377a5c3343f6
Source feed: FDA_Inspections

> FDA Inspection 678543 for DeRoyal Industries Inc on August 26, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 678543
- Company Name: DeRoyal Industries Inc
- Inspection Date: 2010-08-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1019823 - 2017-07-25](https://www.globalkeysolutions.net/records/fda_inspections/deroyal-industries-inc/8888dbd1-f89c-47ef-aa56-69f1bf320e51)

Company: https://www.globalkeysolutions.net/companies/deroyal-industries-inc/5d0a8918-4775-4506-9a04-c72da923a6f4

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