# Duke University Medical Center Duke Hospital North, Durham, NC – FDA Inspections

Source: https://www.keypedia.com/companies/duke-university-medical-center-duke-hospital-north/d6edb935-3f14-4e7c-9e15-0c30f18f9da7

> Inspection records and compliance data for Duke University Medical Center Duke Hospital North in Durham, North Carolina. 8 FDA inspections on record, last inspected May 09, 2024.

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## Details

- Name: Duke University Medical Center Duke Hospital North
- FEI Number: 1074242
- Address Line 1: 2301 Erwin Road, Room 1720
- City: Durham
- State: North Carolina
- Zip Code: 27710
- Country Name: United States
- Address: 2301 Erwin Road, Room 1720, Durham, North Carolina 27710, United States
- Country: United States

## Related Documents

- FDA Inspection 1238536 - Duke University Medical Center Duke Hospital North - 2024-05-09 — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2024
- FDA Inspection 1077870 - Duke University Medical Center Duke Hospital North - 2019-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2019
- FDA Inspection 997958 - Duke University Medical Center Duke Hospital North - 2017-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2017
- FDA Inspection 927957 - Duke University Medical Center Duke Hospital North - 2015-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2015
- FDA Inspection 811549 - Duke University Medical Center Duke Hospital North - 2012-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2012
- FDA Inspection 770870 - Duke University Medical Center Duke Hospital North - 2012-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2012
- FDA Inspection 627540 - Duke University Medical Center Duke Hospital North - 2009-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2009
- FDA Inspection 559303 - Duke University Medical Center Duke Hospital North - 2009-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2009

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