| DESCRIPTION |
+---------------------------------------------------------------+
| The Food and Drug Administration classifies this software as |
| a medical device. As such, it may not be changed in any way. |
| Modifications to this software may result in an adulterated |
| medical device under 21CFR820, the use of which is considered |
| to be a violation of US Federal Statutes. |
| |
+---------------------------------------------------------------+
This file contains a log of media bundles from which study data were
| |
imported by the Importer II application. A media bundle is a group of
studies under a single Importer II work item. A media bundle may or may
not represent a single piece of media or a single network transaction.
This file includes information about media validity, the user who
reconciled the associated studies, etc.
(MAG*3.0*118)
| Property of the US Government. |
| No permission to copy or redistribute this software is given. |
| Use of unreleased versions of this software requires the user |
| to execute a written test agreement with the VistA Imaging |
| Development Office of the Department of Veterans Affairs, |
| telephone (301) 734-0100. |
| |
|
