FDA Inspection 1117585 — Abbott

Abbott — FEI 3005334138

The FDA completed an inspection of Abbott on January 10, 2020 in Plymouth, MN. 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
January 10, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Plymouth, MN (United States)

Additional Details

Sponsor, Contract Research Organization