FDA Inspection 755428 — ABS Corporation

ABS Corporation — FEI 1950042

The FDA completed an inspection of ABS Corporation on December 2, 2011 in Omaha, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 2, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Omaha, NE (United States)

Citations

IDCFRDescription
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1586921 CFR 111.75(c)Specifications met - verify; finished batch