# FDA Inspection 999614 - Michael L. Swank, M.D. - January 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/michael-l-swank-md/0f0817dd-aa5e-4f78-b25f-7a79f787c43d
Source feed: FDA_Inspections

> FDA Inspection 999614 for Michael L. Swank, M.D. on January 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999614
- Company Name: Michael L. Swank, M.D.
- Inspection Date: 2017-01-19
- 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/michael-l-swank-md/f577e1cb-80f1-4a81-872b-88da0674bc5e

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