Beth Israel Deaconess Medical Center Angiographic Core Lab FDA Record
- Latest inspection NAI · Sep 24, 2015
- No warning letters matched by name
Beth Israel Deaconess Medical Center Angiographic Core Lab has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Beth Israel Deaconess Medical Center Angiographic Core Lab" is on file.
- Latest inspection
- Sep 24, 2015 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 3 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 24, 2015 | Boston, MA | Devices | No Action Indicated (NAI) | 3008767943 |
| Aug 4, 2011 | Boston, MA | Devices | No Action Indicated (NAI) | 3008767943 |
| Apr 14, 2011 | Boston, MA | Devices | No Action Indicated (NAI) | 3008767943 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3008767943 | Boston, MA | 3 | Sep 24, 2015 |
Beth Israel Deaconess Medical Center Angiographic Core Lab and the FDA: common questions
Has Beth Israel Deaconess Medical Center Angiographic Core Lab received an FDA warning letter?
No FDA warning letter addressed to the name "Beth Israel Deaconess Medical Center Angiographic Core Lab" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Beth Israel Deaconess Medical Center Angiographic Core Lab received an FDA Form 483?
FDA has not published a Form 483 for "Beth Israel Deaconess Medical Center Angiographic Core Lab" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Beth Israel Deaconess Medical Center Angiographic Core Lab?
The most recent FDA inspection on file ended Sep 24, 2015 at Boston, MA and was classified NAI. FDA has 3 inspections of Beth Israel Deaconess Medical Center Angiographic Core Lab on file.
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