FDA Inspection 820210 — Abbott Diagnostics Scarborough, Inc.

Abbott Diagnostics Scarborough, Inc. — FEI 1221359

The FDA completed an inspection of Abbott Diagnostics Scarborough, Inc. on February 1, 2013 in Scarborough, ME. 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 1, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Scarborough, ME (United States)

Additional Details

Postmarket Audit Inspections