FDA Inspection 627906 — Abbott

Abbott — FEI 3005334138

The FDA completed an inspection of Abbott on Nov 17, 2009 in Plymouth, MN. 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
Nov 17, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Plymouth, MN (United States)

Additional Details

Sponsor, Contract Research Organization

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