# FDA Inspection 953519 - Aquilla Turk, MD - December 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/aquilla-turk-md/1ab14e85-e625-47cf-a6e8-329657330f3c
Source feed: FDA_Inspections

> FDA Inspection 953519 for Aquilla Turk, MD on December 10, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953519
- Company Name: Aquilla Turk, MD
- Inspection Date: 2015-12-10
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/aquilla-turk-md/d4268182-48a0-4c6e-bbd2-df2c308869d9

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