BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action for the Optiplex Borrelia IgM Test, Diamex

Product group In-vitro diagnostics - microbiological products
Reference 01039/14

Corrective action from Diamex for the Optiplex Borrelia IgM Test due to invalid results. Customers were informed accordingly.

Corrective action for the Optiplex Borrelia IgM Test, Diamex , Download_VeroeffentlichtAm_EN PDF, 35KB, File does not meet accessibility standards