| 000 | 01542nam a2200397 i 4500 | ||
|---|---|---|---|
| 001 | ocn961477237 | ||
| 003 | OCoLC | ||
| 005 | 20170208053817.0 | ||
| 006 | m o d f | ||
| 007 | cr mn||||||||| | ||
| 008 | 161031s2009 mdua ob f000 0 eng c | ||
| 040 |
_aGPO _beng _erda _epn _cGPO |
||
| 042 | _apcc | ||
| 043 | _an-us--- | ||
| 074 | _a0445-B-07 (online) | ||
| 086 | 0 | _aHE 1.75:OEI-01-08-00110 | |
| 088 | _aOEI-01-08-00110 | ||
| 099 | _aHE 1.75:OEI-01-08-00110 | ||
| 110 | 1 |
_aUnited States. _bDepartment of Health and Human Services. _bOffice of Inspector General, _eauthor. |
|
| 245 | 1 | 0 | _aAdverse event reporting for medical devices. |
| 246 | 1 |
_iRunning title: _aAdverse event reporting for medical devices |
|
| 264 | 1 |
_a[Washington, D.C.] : _bDepartment of Health and Human Services, Office of Inspector General, _c2009. |
|
| 300 |
_a1 online resource (iv, 29 pages) : _billustrations |
||
| 337 | _2rdamedia | ||
| 338 | _2rdacarrier | ||
| 588 | _aDescription based on online resource; title from PDF title page (HHS, viewed Oct. 28, 2016). | ||
| 500 | _a"October 2009." | ||
| 500 | _a"OEI-01-08-00110." | ||
| 500 | _aCRDP Project record. | ||
| 504 | _aIncludes bibliographical references. | ||
| 650 | 0 |
_aProducts liability _xMedical instruments and apparatus _xReporting _zUnited States. |
|
| 610 | 2 | 0 | _aCenter for Devices and Radiological Health (U.S.) |
| 650 | 0 |
_aConsumer protection _zUnited States. |
|
| 856 | 4 | 0 | _uhttp://purl.fdlp.gov/GPO/gpo73890 |
| 949 |
_aBEV _bFed Docs |
||
| 999 |
_c257201 _d257201 |
||