FDA Inspection 1258987 — Microvention, Inc.

Microvention, Inc. — FEI 3003523199

The FDA completed an inspection of Microvention, Inc. on January 8, 2025 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 8, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aliso Viejo, CA (United States)

Additional Details

Sponsor, Contract Research Organization