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26 Jan 2007, 10:43 am
About Mimosa Mimosa Systems, Inc. delivers next-generation information management solutions for information immediacy, discovery and continuity. [read post]
31 Oct 2012, 10:39 am by Rebecca Tushnet
KTurbo, Inc., --- F.3d ----, 2012 WL 4856489 (7th Cir.) [read post]
16 May 2019, 5:38 am by Green, Schafle & Gibbs
In order to conceal the purpose of the withdrawal, Donnelly submitted a wire transfer form to the firm that inaccurately described the reason for the wire as for a car purchase. [read post]
1 Nov 2017, 12:45 pm by James Innocent
However, stream of commerce theory says that “an entity that participates in placing a defective product in the general marketplace is strictly liable for harm caused by the product. [read post]
16 May 2012, 11:58 pm
A manufacturing defect, which generally occurs when an otherwise safe product is assembled carelessly; 2. [read post]
17 Jan 2009, 9:52 am
BG successfully merged with Banco Continental (BC), integrating its customers, employees and products in less than nine months. [read post]
26 Sep 2010, 10:08 pm by Marie Louise
WM Wrigley (Peter Zura’s 271 Patent Blog) District Court E D Texas: Domestic use of foreign product manufactured using patented method is not an act of infringement: Input/Output, Inc. et al v. [read post]
25 Oct 2019, 6:15 am by Abigail Court (Toronto)
The post Digging for a Solution: alternative sources of financing in the mining sector appeared first on Deal Law Wire. [read post]
28 Sep 2010, 3:14 pm by Kelly
Par Pharmaceutical, Inc; Schering-Plough Healthcare Products, Inc. et al. v. [read post]
16 Jul 2021, 7:46 am by Eric Goldman
Everest for Faking Photo * Wired: How Covid Gums Up the Court System * Les Giblin LLC v. [read post]
7 Jun 2009, 5:56 am
  In the absence of such a clause the refusal to handle products or services declared hot does contravene the Code. [read post]
9 Aug 2010, 12:58 am by Kelly
Global Global – General Corporate business leaders: Want to create value from your IP? [read post]
30 Oct 2007, 3:44 pm
  Nor does the FDA require studies of medical devices after market release, as a general rule. [read post]