FDA Inspection 888754 — Ulrich Gmbh & Co. KG

Ulrich Gmbh & Co. KG — FEI 3002807156

The FDA completed an inspection of Ulrich Gmbh & Co. KG on Jul 10, 2014 in Ulm. 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 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Ulm (Germany)

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