FDA Inspection 1074516 — Abbott Diagnostics Scarborough, Inc.

Abbott Diagnostics Scarborough, Inc. — FEI 1221359

The FDA completed an inspection of Abbott Diagnostics Scarborough, Inc. on Nov 30, 2018 in Scarborough, ME. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 30, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Scarborough, ME (United States)

Additional Details

Sponsor, Contract Research Organization

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