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U.S. Department of Health and Human Services

Import Refusal Report

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Refusal Actions by FDA as Recorded in OASIS

for 57-Bio & Licensed In-Vivo & In-Vitro Diag


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
233-3142779-1/1/1 26-Sep-2003 57CY02 3002806949 Novartis Vaccines and Diagnostics Limited United Kingdom
 
112-1372232-5/1/1 29-Sep-2003 57OH01 3003828812 Hans Biomed Corporation Korea, Republic Of (South)
 
112-1136262-9/1/1 12-Sep-2003 57YY99 3002688594 Mikrogen Gmbh Germany
 
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