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FDA Inspection 596016 — ABS Corp

ABS Corp — FEI 3002675394

The FDA completed an inspection of ABS Corp on Jul 9, 2009 in Minnetonka, 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
Jul 9, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)

Facility

Other inspections at this facility

FDA data resources

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