# FDA Inspection 1200527 - LASERNEEDLE GMBH - March 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/laserneedle-gmbh/11a499e2-3d5f-428e-9e2f-0a58441aab2b
Source feed: FDA_Inspections

> FDA Inspection 1200527 for LASERNEEDLE GMBH on March 23, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200527
- Company Name: LASERNEEDLE GMBH
- Inspection Date: 2023-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200527 - 2023-03-23](https://www.keypedia.com/records/fda_inspections/laserneedle-gmbh/7679bd79-16ed-42c5-8640-32b162f3b1c7)

Company: https://www.keypedia.com/companies/laserneedle-gmbh/e079c182-51d7-4880-9948-837fa62c7579

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