FDA Inspection 1077480 — Microvention, Inc.

Microvention, Inc. — FEI 3003523199

The FDA completed an inspection of Microvention, Inc. on January 17, 2019 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
January 17, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aliso Viejo, CA (United States)

Additional Details

Sponsor, Contract Research Organization