FDA Inspection 752842 — Regenesis Biomedical Inc

Regenesis Biomedical Inc — FEI 3003070149

The FDA completed an inspection of Regenesis Biomedical Inc on November 9, 2011 in Scottsdale, AZ. 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 9, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Scottsdale, AZ (United States)