# DeRoyal Industries, Inc. – FDA Inspection, Sep 26, 2012

Source: https://www.keypedia.com/records/fda_inspections/deroyal-industries-inc/66f699f8-0bd5-4f11-8c15-59b49c53c0b9
Source feed: FDA_Inspections

> FDA inspection 800786 of DeRoyal Industries, Inc., September 26, 2012. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800786
- Company Name: DeRoyal Industries, Inc.
- Inspection Date: 2012-09-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 880853 - 2014-05-22](https://www.keypedia.com/records/fda_inspections/deroyal-industries-inc/fc515e22-56de-48ac-8ee2-0e8abadf9f5f)
- [FDA Inspection 601489 - 2009-07-31](https://www.keypedia.com/records/fda_inspections/deroyal-industries-inc/7a15b788-ad21-422f-b6f5-052af0662734)

Company: https://www.keypedia.com/companies/deroyal-industries-inc/bd9bb0f2-5afb-463e-8035-08d1979727ec

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