# FDA Inspection 1201351 - Melanie Palm, MD - February 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/melanie-palm-md/201a1319-c916-4668-9525-ed62fd3e4ba2
Source feed: FDA_Inspections

> FDA Inspection 1201351 for Melanie Palm, MD on February 23, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201351
- Company Name: Melanie Palm, MD
- Inspection Date: 2023-02-23
- 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/melanie-palm-md/6e780829-9516-4322-8597-87db115289ac

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