# FDA Inspection 1199271 - MELOQ AB - March 09, 2023

Source: https://www.keypedia.com/records/fda_inspections/meloq-ab/bfe5cd46-4daf-43ae-84c8-0bc8ec4cbe9f
Source feed: FDA_Inspections

> FDA Inspection 1199271 for MELOQ AB on March 09, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199271
- Company Name: MELOQ AB
- Inspection Date: 2023-03-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199271 - 2023-03-09](https://www.keypedia.com/records/fda_inspections/meloq-ab/30a75e5e-dc17-4299-9ca5-822eedb64c87)

Company: https://www.keypedia.com/companies/meloq-ab/1e07d5d9-24f4-4959-9418-342e85d99b37

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