FDA Inspection
LASER LIPO LIMITEDLASER LIPO LIMITED – FDA Inspection, Jul 5, 2013
Record Details
This FDA Inspection record concerns LASER LIPO LIMITED, with an inspection on July 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LASER LIPO LIMITED
- Inspection Date
- July 5, 2013
- Product Type
- Devices
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ID · 3fbbb405-1cb7-49f3-a101-ceb2e3984bfc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 844981
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.2(b)Abbreviated requirements / non-significant risk study
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Other FDA inspections of LASER LIPO LIMITED
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 18, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 15, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for LASER LIPO LIMITED
- FDA Inspection 1179878 - 2022-08-18
- FDA Inspection 1014457 - 2017-06-15
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