# FDA Inspection 1026433 - Dornier Medtech Laser GmbH - July 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/dornier-medtech-laser-gmbh/35cd56e7-52e7-4ada-8d08-72b7b3dd8023
Source feed: FDA_Inspections

> FDA Inspection 1026433 for Dornier Medtech Laser GmbH on July 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026433
- Company Name: Dornier Medtech Laser GmbH
- Inspection Date: 2017-07-20
- 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 1026433 - 2017-07-20](https://www.keypedia.com/records/fda_inspections/dornier-medtech-laser-gmbh/4f8f6a95-a6e9-49e9-90cf-24f639c0b988)
- [FDA Inspection 1026433 - 2017-07-20](https://www.keypedia.com/records/fda_inspections/dornier-medtech-laser-gmbh/89905778-3885-4ae4-93ec-a225e0b0cb62)
- [FDA Inspection 892024 - 2014-07-31](https://www.keypedia.com/records/fda_inspections/dornier-medtech-laser-gmbh/7b00e03b-e131-45ee-b4a2-b0fdee19b48c)
- [FDA Inspection 892024 - 2014-07-31](https://www.keypedia.com/records/fda_inspections/dornier-medtech-laser-gmbh/8cdafc06-08b7-4464-b21b-7ede526bb788)

Company: https://www.keypedia.com/companies/dornier-medtech-laser-gmbh/b3c49e86-b193-4769-a741-7380dfd1d764

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