Turbare Manufacturing Form 483 Details
Form 483Source: FDA, document on fileFDA released the Form 483 itself and the document linked above is FDA's own file, served from fda.gov.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3027507354.
Turbare Manufacturing
Arkansas
Issue DateMay 07, 2026
FEI Number3027507354
CountryUnited States
Status
1 Related Warning LetterEstablishment Type
Outsourcing Facility