|
|
|
|
|
|
|
|
1. |
Record Nr. |
UNINA9910699069003321 |
|
|
Autore |
Crosse Marcia |
|
|
Titolo |
Medical devices [[electronic resource] ] : shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives / / statement of Marcia Crosse |
|
|
|
|
|
|
|
Pubbl/distr/stampa |
|
|
[Washington, D.C.] : , : U.S. Govt. Accountability Office, , [2009] |
|
|
|
|
|
|
|
Descrizione fisica |
|
1 online resource (18 pages) : illustrations |
|
|
|
|
|
|
Collana |
|
Testimony ; ; GAO-09-370T |
|
|
|
|
|
|
Soggetti |
|
Medical instruments and apparatus industry - United States |
Medical instruments and apparatus - Inspection - United States |
Risk assessment - Government policy - United States |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Note generali |
|
Title from title screen (GAO, viewed July 22, 2009). |
"For release ... June 18, 2009." |
|
|
|
|
|
|
|
|
Nota di bibliografia |
|
Includes bibliographical references. |
|
|
|
|
|