# Ducommun Labarge Technologies – FDA Inspection, Aug 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/ducommun-labarge-technologies/8aaa74d9-1543-4fa9-a25d-12d99152898c
Source feed: FDA_Inspections

> FDA inspection 1022305 of Ducommun Labarge Technologies, August 11, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022305
- Company Name: Ducommun Labarge Technologies
- Inspection Date: 2017-08-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1274180 - 2025-06-27](https://www.keypedia.com/records/fda_inspections/ducommun-labarge-technologies/867c8c8c-4b26-486a-9a0a-885e3ca956ec)
- FDA Inspection 887596 - 2014-07-17

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/ducommun-labarge-technologies/9f552cb3-d285-4b49-a1ee-d9adbd6ba6d7

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