FDA Inspection 830029 — MICROVENTION INC.

MICROVENTION INC. — FEI 3013556777

The FDA completed an inspection of MICROVENTION INC. on Apr 30, 2013 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
Apr 30, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Aliso Viejo, CA (United States)

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