# Sligh, Teresa S. MD – FDA Inspection, Mar 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/sligh-teresa-s-md/615b6dd3-d590-4823-b641-ee9b4637c54e
Source feed: FDA_Inspections

> FDA inspection 650262 of Sligh, Teresa S. MD, March 01, 2010. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 650262
- Company Name: Sligh, Teresa S. MD
- Inspection Date: 2010-03-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1165847 - 2022-03-28
- [FDA Inspection 962369 - 2016-03-01](https://www.keypedia.com/records/fda_inspections/sligh-teresa-s-md/7b994709-d8ad-45a5-94e4-b2c5a681ee54)
- FDA Inspection 928743 - 2015-06-04

Company: https://www.keypedia.com/companies/sligh-teresa-s-md/3c8ed996-408f-4b9c-b58d-33ea24b73847

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