| 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 maps retention policies, via an acquisition location, to the
storage providers that should be used to satisfy that retention policy.
| |
In a valid configuration, the attributes on the retention policy (i.e
Minimum Archive Copies, etc) can be matched to the corresponding attributes
of the mapped storage provider (i.e. Archive), to see whether the configuration
is valid.
This file also holds a flag indicating whether a particular provider
should be called synchronously or asynchronously.
| 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. |
| |
|
