# FDA Inspection 944715 - Wavelight GmbH - September 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/wavelight-gmbh/b2955f2f-c352-428e-9f01-ad5ea82c855f
Source feed: FDA_Inspections

> FDA Inspection 944715 for Wavelight GmbH on September 11, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 944715
- Company Name: Wavelight GmbH
- Inspection Date: 2015-09-11
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 944715 - 2015-09-11](https://www.keypedia.com/records/fda_inspections/wavelight-gmbh/a70de369-3103-4912-8757-0fb94c899cd8)
- [FDA Inspection 819586 - 2013-01-31](https://www.keypedia.com/records/fda_inspections/wavelight-gmbh/e02d01a9-80cc-41fe-ba00-f80b4a4aedb0)

Company: https://www.keypedia.com/companies/wavelight-gmbh/739a03a6-2309-457b-95db-ff049713a6ef

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