FDA Inspection 903595 — Straumann USA LLC

Straumann USA LLC — FEI 1000121052

The FDA completed an inspection of Straumann USA LLC on November 13, 2014 in Andover, MA. 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
November 13, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Andover, MA (United States)