# FDA Inspection 1101500 - Ralph A. Liebelt, M.D. - August 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/ralph-a-liebelt-md/56c67bdc-1de8-4702-951c-7f31dea773d4
Source feed: FDA_Inspections

> FDA Inspection 1101500 for Ralph A. Liebelt, M.D. on August 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101500
- Company Name: Ralph A. Liebelt, M.D.
- Inspection Date: 2019-08-21
- 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/ralph-a-liebelt-md/d48b36ea-782a-4190-ab4a-52471a932e14

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