483
CenexiFDA 483 - Cenexi
Record Details
An FDA inspection of Guerbet in Osny, France, identified one observation related to incomplete cleaning validation for a machine. The firm had not fully executed the required protocols, specifically missing a critical observation step. This indicates a deficiency in the firm's quality control processes for equipment maintenance.
- Company
- Cenexi
- Product Type
- Other
- Person
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ID · 14789f2d-8738-46fa-9e1b-b32d11a53c82