FDA Inspection 712776 — STRATEC SE

STRATEC SE — FEI 3003413192

The FDA completed an inspection of STRATEC SE on February 10, 2011 in Birkenfeld. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 10, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Birkenfeld (Germany)