Drug and Food Administration. ‘We’re being extremely methodical in bringing this technology to the clinic, while ensuring that the equipment meets the laboratories’ desires.’ The Infinity Series1200 is stated in Waldbronn, Germany, and the 6000 Series is manufactured in Singapore. Both facilities are registered as medical gadget establishments with the FDA, a requirement for manufacturing medical devices. In September 2011, those facilities were certified as conference the internationally known ISO 13485 quality-management standard. In June 2011, Agilent’s reagent manufacturing facility in Cedar Creek, Texas, was authorized with the FDA as a medical gadget establishment.. Agilent’s liquid chromatography and mass spec systems listed as Class I medical products with FDA Agilent Technology Inc.The recall totals about 23,000 pounds of food, according to the U.S. Section of Agriculture’s Food Basic safety and Inspection Service. Expiration dates range from 10/23/13 to 3/17/14 – – a complete list of products and UPC codes can be found on Reser’s website. Reser’s Good Foods is based in Beaverton, Ore., however the products in question were produced at a Topeka, Kan. Processing plant. The issue was discovered through examining conducted by the Canadian Food Inspection Agency. A traceback investigation and follow-up tests by FDA at the service determined there was potential cross contamination of products with listeria from item contact surfaces.