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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AMO MFG, USA, LLC

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AMO MFG, USA, LLC Back to Search Results
Event Type  Injury  
Manufacturer Narrative

Unable to evaluate, info is not available to identify the device or reporter.

 
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Manufacturer (Section G)
AMO MFG, USA, LLC
510 cottonwood dr
milpitas CA 92705 493
Manufacturer Contact
carol kail
1700 e. st. andrew pl
santa ana , CA 92705-4933
7142478598
MDR Report Key1088283
Report Number3006695864-2008-00009
Device Sequence Number1
Product CodeLZS
Report Source Manufacturer
Source Type Other
Type of Report Initial
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received07/28/2008
Was the Report Sent to FDA? No
Date Manufacturer Received06/30/2008
Was Device Evaluated By Manufacturer? No
Is The Device Single Use? No
Type of Device Usage Unkown

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