# Novant Health Presbyterian Medical Center, Charlotte, NC – FDA Inspections

Source: https://www.keypedia.com/companies/novant-health-presbyterian-medical-center/cedc77c1-9de1-4b56-a11b-00e17c11b346

> Inspection records and compliance data for Novant Health Presbyterian Medical Center in Charlotte, North Carolina. 7 FDA inspections on record, 1 Form 483, last inspected September 12, 2024.

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## Details

- Name: Novant Health Presbyterian Medical Center
- FEI Number: 1076873
- Address Line 1: 200 Hawthorne Ln
- City: Charlotte
- State: North Carolina
- Zip Code: 28204
- Country Name: United States
- Address: 200 Hawthorne Ln, Charlotte, North Carolina 28204, United States
- Country: United States

## Related Documents

- FDA Inspection 1249457 - Novant Health Presbyterian Medical Center - 2024-09-12 — source: FDA, date: September 12, 2024
- FDA Inspection 1249457 - Novant Health Presbyterian Medical Center - 2024-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2024
- FDA Inspection 1092723 - Novant Health Presbyterian Medical Center - 2019-05-24 — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2019
- [FDA Inspection 1023386 - Novant Health Presbyterian Medical Center - 2017-08-25](https://www.keypedia.com/records/fda_inspections/novant-health-presbyterian-medical-center/bdafeb33-fb0d-474d-8c7a-b68bd1ca5214) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 25, 2017
- FDA Inspection 927016 - Novant Health Presbyterian Medical Center - 2015-05-19 — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2015
- FDA Inspection 814376 - Novant Health Presbyterian Medical Center - 2013-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2013
- FDA Inspection 720828 - Novant Health Presbyterian Medical Center - 2011-04-14 — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2011
- FDA Inspection 573057 - Novant Health Presbyterian Medical Center - 2009-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2009

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