# FDA Inspection 1274180 - Ducommun Labarge Technologies - June 27, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/6bf286ef-b62d-4c79-924b-4e2d30c2d9d4
Source feed: FDA_Inspections

> FDA Inspection 1274180 for Ducommun Labarge Technologies on June 27, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274180
- Company Name: Ducommun Labarge Technologies
- Inspection Date: 2025-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1274180 - 2025-06-27](https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/1da84e04-25ea-452d-beab-7ddcb4bb9666)
- [FDA Inspection 1274180 - 2025-06-27](https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/867c8c8c-4b26-486a-9a0a-885e3ca956ec)
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- [FDA Inspection 1022305 - 2017-08-11](https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/83d79da1-589a-449c-8e37-2bfd73f2f8d3)
- [FDA Inspection 1022305 - 2017-08-11](https://www.globalkeysolutions.net/records/fda_inspections/ducommun-labarge-technologies/44bb7ce5-060a-4b81-b1a1-881a78506770)

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