FDA Inspection 1060483 — Cytori Therapeutics, Inc.

Cytori Therapeutics, Inc. — FEI 3002642958

The FDA completed an inspection of Cytori Therapeutics, Inc. on Jun 19, 2018 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 19, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)