FDA Inspection
Wavelight GmbHWavelight GmbH – FDA Inspection, Jan 31, 2013
Record Details
This FDA Inspection record concerns Wavelight GmbH, with an inspection on January 31, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Wavelight GmbH
- Inspection Date
- January 31, 2013
- Product Type
- Devices
View Company Profile
ID · e02d01a9-80cc-41fe-ba00-f80b4a4aedb0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819586
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Wavelight GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2015 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Wavelight GmbH
- FDA Inspection 944715 - 2015-09-11
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