# FDA Inspection 739973 - Beth Israel Deaconess Medical Center Angiographic Core Lab - August 04, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/beth-israel-deaconess-medical-center-angiographic-core-lab/3f31b8aa-1016-4158-9d69-7b3262cc2f31
Source feed: FDA_Inspections

> FDA Inspection 739973 for Beth Israel Deaconess Medical Center Angiographic Core Lab on August 04, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 739973
- Company Name: Beth Israel Deaconess Medical Center Angiographic Core Lab
- Inspection Date: 2011-08-04
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 944356 - 2015-09-24](https://www.globalkeysolutions.net/records/fda_inspections/beth-israel-deaconess-medical-center-angiographic-core-lab/db244bf6-449b-4119-a279-c3a5647f7ac3)
- [FDA Inspection 721111 - 2011-04-14](https://www.globalkeysolutions.net/records/fda_inspections/beth-israel-deaconess-medical-center-angiographic-core-lab/e499dafc-1e51-48ee-a668-1d90632d35c8)

Company: https://www.globalkeysolutions.net/companies/beth-israel-deaconess-medical-center-angiographic-core-lab/20d761cd-2639-47e0-93e5-7cad51bb22aa

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
