FDA Inspection 820210 — Abbott Diagnostics Scarborough, Inc.

Abbott Diagnostics Scarborough, Inc. — FEI 1221359

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.