FDA Inspection 851671 — Instrumed GmbH

Instrumed GmbH — FEI 3007290840

The FDA completed an inspection of Instrumed GmbH on Aug 1, 2013 in Tuttlingen. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Aug 1, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)

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