# FDA Inspection 1290416 - MOWI - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/mowi/6c71c810-9d5e-41a8-9438-7a09f2961058
Source feed: FDA_Inspections

> FDA Inspection 1290416 for MOWI on October 30, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290416
- Company Name: MOWI
- Inspection Date: 2025-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1084018 - 2019-03-27](https://www.keypedia.com/records/fda_inspections/mowi/39257d59-d027-457a-a00c-f055ed92b540)
- [FDA Inspection 1084018 - 2019-03-27](https://www.keypedia.com/records/fda_inspections/mowi/65e3bf61-d64a-437f-a69e-f298bd405d07)

Company: https://www.keypedia.com/companies/mowi/e6cc00ce-c8d7-458a-b77b-22b2c30476e8

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