FDA Inspection 799436 — Abbott Laboratories Vascular Enterprises Ltd.

Abbott Laboratories Vascular Enterprises Ltd. — FEI 3003309939

The FDA completed an inspection of Abbott Laboratories Vascular Enterprises Ltd. on September 20, 2012 in Beringen. 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
September 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Beringen (Switzerland)