FDA yepamutemo webhusaiti yekubvunza link:
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm
Iyo inotevera skrini inobuda:
1. Mushure mekupinda FDA kunyoresa uye certification peji, rutivi rworuboshwe ndiro zita rebhizimisi uye kodhi yechigadzirwa, nezvimwewo, semuenzaniso, "Kugadzwa kana Zita rekutengeserana", unogona kuisa zita rechiChirungu rebhizimisi kuti ubvunze.
2. Rutivi rwekurudyi nderekushandisa FDA Registration nhamba yebhizinesi kubvunza ruzivo rwebhizinesi rakanyoreswa, seKunyoresa kana FEI Nhamba, izvo zvinoda kuti bhizinesi rekunyoresa nhamba kubvunza.
Pinda "Foosin"Kutsvaga nekukurumidza: Dzvanya Tsvaga pakona yekurudyi kuti uise inotevera skrini:
Ipapo iwe unogona kuona iyo FDA ruzivo rwezvese zvigadzirwa zveFoosin
Nguva yekutumira: Jun-06-2022