# FDA Inspection 1220148 - Remeda AB - September 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/remeda-ab/0a7b7afe-87c1-49c9-ba8a-bb8d75a4aa54
Source feed: FDA_Inspections

> FDA Inspection 1220148 for Remeda AB on September 14, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1220148
- Company Name: Remeda AB
- Inspection Date: 2023-09-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/remeda-ab/ebd3fd12-2e45-4db1-ac11-1ddbc695a7c7

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