Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1950042.
Observations2
Issue DateDecember 02, 2011
Status1 Related Warning Letter
Related Inspections10
Establishment Details
Firm
ABS Corporation
Location
Omaha, Nebraska, United States
FEI Number
1950042
Product Type
Devices
Issue Date
December 02, 2011
Country
United States
Inspection History, 2014 to 2026
NAI6
VAI3
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.