FDA Inspection 629675 — Microvention, Inc.

Microvention, Inc. — FEI 3003523199

The FDA completed an inspection of Microvention, Inc. on November 20, 2009 in Aliso Viejo, 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
November 20, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Aliso Viejo, CA (United States)