FDA Inspection 666601 — Cytori Therapeutics, Inc.

Cytori Therapeutics, Inc. — FEI 3002642958

The FDA completed an inspection of Cytori Therapeutics, Inc. on Jun 18, 2010 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 18, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)