FDA Inspection 844893 — Cytori Therapeutics, Inc.

Cytori Therapeutics, Inc. — FEI 3002642958

The FDA completed an inspection of Cytori Therapeutics, Inc. on Jul 26, 2013 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures