{"product_id":"fda-483-response-for-patheon-thermo-fisher-inspection-related-eir-and-inspection-classification-letter-fei-1018495-inspection-may-15-24-2024","title":"FDA 483 Response for Patheon\/Thermo Fisher Inspection – Related EIR and inspection classification letter, FEI: 1018495, Inspection: May 15-24, 2024.","description":"\u003cb\u003eOriginal Request:\u003c\/b\u003e  I am requesting a copy of the firm’s 483 response related to the inspection that took place at Patheon\/Thermo Fisher in Greenville, NC, as well as the related EIR and inspection classification letter issued thereto.   FEI Number: 1018495 Date: May 15-24, 2024 Product Type: Human drugs Please provide the documents electronically if possible.","brand":"FDA","offers":[{"title":"Default Title","offer_id":50860941213860,"sku":"FDAFT806","price":89.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-483-response-for-patheon-thermo-fisher-inspection-related-eir-and-inspection-classification-letter-fei-1018495-inspection-may-15-24-2024","provider":"FOIA Document Source","version":"1.0","type":"link"}