FDA Inspection 543742 — Cellestis Inc

Cellestis Inc — FEI 3003964343

The FDA completed an inspection of Cellestis Inc on October 6, 2008 in Santa Clarita, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 6, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clarita, CA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation