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FDA Inspection 699615 — BioSculptor Corporation

BioSculptor Corporation — FEI 1000560772

The FDA completed an inspection of BioSculptor Corporation on November 30, 2010 in Hialeah, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 30, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hialeah, FL (United States)

Facility

Other inspections at this facility

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  • 1120660 (NAI Fri Mar 13 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 945758 (NAI Tue Oct 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 739588 (VAI Tue Aug 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 699614 (VAI Tue Nov 30 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources