# Wavelight GmbH – FDA Inspection, Jan 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/wavelight-gmbh/e02d01a9-80cc-41fe-ba00-f80b4a4aedb0
Source feed: FDA_Inspections

> FDA inspection 819586 of Wavelight GmbH, January 31, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819586
- Company Name: Wavelight GmbH
- Inspection Date: 2013-01-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 944715 - 2015-09-11

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