FDA Inspection 956472 — Jarit GmbH

Jarit GmbH — FEI 3005809810

The FDA completed an inspection of Jarit GmbH on Jan 19, 2016 in Rietheim-Weilheim. 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
Jan 19, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rietheim-Weilheim (Germany)

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