FDA Inspection 674766 — Magstim Inc

Magstim Inc — FEI 3001090553

The FDA completed an inspection of Magstim Inc on Aug 12, 2010 in Eugene, OR. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 12, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Eugene, OR (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

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