{"product_id":"fda-form-483-meridian-medical-technologies-llc-inspection-saint-louis-12-21-2019-fei-1950222","title":"FDA Form 483 – Meridian Medical Technologies, LLC Inspection (Saint Louis, 12\/21\/2019, FEI 1950222)","description":"\u003cb\u003eRequest Contents:\u003c\/b\u003e FDA Form 483 for Meridian Medical Technologies, LLC, a subsidiary of Kindeva Drug Delivery, L.P. Inspection ended on Dec 21, 2019, for the Saint Louis, United States site (FEI 1950222). Inspection related to Medical Devices and Rad Health.","brand":"FDA","offers":[{"title":"Default Title","offer_id":50787182805156,"sku":"FDAFT229","price":89.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-form-483-meridian-medical-technologies-llc-inspection-saint-louis-12-21-2019-fei-1950222","provider":"FOIA Document Source","version":"1.0","type":"link"}