FDA Inspection 1077480 — MICROVENTION INC.

MICROVENTION INC. — FEI 3013556777

The FDA completed an inspection of MICROVENTION INC. on Jan 17, 2019 in Aliso Viejo, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 17, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aliso Viejo, CA (United States)

Additional details

Sponsor, Contract Research Organization

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.