FDA Inspection 823584 — Silimed Industria De Implantes Ltda

Silimed Industria De Implantes Ltda — FEI 3002808187

The FDA completed an inspection of Silimed Industria De Implantes Ltda on Mar 14, 2013 in Rio De Janeiro. 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
Mar 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Rio De Janeiro (Brazil)

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