FDA Inspection 885777 — Medeologix LLC

Medeologix LLC — FEI 3008791915

The FDA completed an inspection of Medeologix LLC on Jul 2, 2014 in San Jose, 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
Jul 2, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

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