# FDA Inspection 1199980 - Vasorum Limited - January 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/vasorum-limited/5cc912c5-6c8d-472f-8e70-5f3fa00f229a
Source feed: FDA_Inspections

> FDA Inspection 1199980 for Vasorum Limited on January 26, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199980
- Company Name: Vasorum Limited
- Inspection Date: 2023-01-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1030840 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/vasorum-limited/74796de2-55cd-4ce6-a524-3e11cdf36a75)
- [FDA Inspection 1030840 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/vasorum-limited/220770a1-a037-492c-b0e2-3cd6291152c8)
- [FDA Inspection 1030840 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/vasorum-limited/2c35a330-2fab-498a-b5ef-64a3c3af7ee2)

Company: https://www.keypedia.com/companies/vasorum-limited/2a4edaf0-1190-444f-a4cb-1295eecdeb62

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