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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 85-Obstetrical & Gynecological


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
310-8839222-5/1/1 09-Aug-2007 85HIF 3006299427 Cardia Innovation Ab United States
 
112-7445714-4/1/1 31-Aug-2007 85HIS 2642 Okamoto Industries Inc Japan
 
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