FDA Inspection
LASER LIPO LIMITEDLASER LIPO LIMITED – FDA Inspection, Jun 15, 2017
Record Details
This FDA Inspection record concerns LASER LIPO LIMITED, with an inspection on June 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a1ea7205-b01b-4c5a-b38b-bf7e174af71c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1014457
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
- 21 CFR 803.17Lack of Written MDR Procedures
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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 |
| July 5, 2013 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for LASER LIPO LIMITED
- FDA Inspection 1179878 - 2022-08-18
- FDA Inspection 844981 - 2013-07-05
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