FDA Inspection 744683 — Cellestis Inc

Cellestis Inc — FEI 3003964343

The FDA completed an inspection of Cellestis Inc on September 15, 2011 in Santa Clarita, CA. 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
September 15, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clarita, CA (United States)