FDA Inspection 721111 — Beth Israel Deaconess Medical Center Angiographic Core Lab
The FDA completed an inspection of Beth Israel Deaconess Medical Center Angiographic Core Lab on Apr 14, 2011 in Boston, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 14, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Boston, MA (United States)
Additional details
Sponsor, Contract Research Organization