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 rworudyi ndere kushandisa FDA Registration nhamba yebhizimisi kubvunza ruzivo rwekambani yakanyoreswa, yakadai seKunyoresa kana Nhamba yeFEI, iyo inoda nhamba yekunyoresa bhizinesi 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