Genlbet Biopbarmaceuticals SA Form 483 Details

Form 483

Source: 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 3011160795.

Genlbet Biopbarmaceuticals SA

Issue DateJanuary 31, 2023

FEI Number3011160795

CountryN/A

Status

No Warning Letter

Establishment Type

Drug Substance/Drug Product Manufacturer