# FDA Inspection 1022305 - Ducommun Labarge Technologies - August 11, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/83d79da1-589a-449c-8e37-2bfd73f2f8d3
Source feed: FDA_Inspections

> FDA Inspection 1022305 for Ducommun Labarge Technologies on August 11, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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