# Curium Netherlands B.V. – FDA Inspection, Jun 13, 2024

Source: https://www.keypedia.com/records/fda_inspections/curium-netherlands-bv/0343b087-e460-4ce9-a1d0-2c9384bda003
Source feed: FDA_Inspections

> FDA inspection 1243632 of Curium Netherlands B.V., June 13, 2024. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1243632
- Company Name: Curium Netherlands B.V.
- Inspection Date: 2024-06-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1320892 - 2024-05-17
- FDA Inspection 1129626 - 2020-01-16
- [FDA Inspection 1056705 - 2018-06-01](https://www.keypedia.com/records/fda_inspections/curium-netherlands-bv/f6284b7e-80c2-4591-b5aa-65fbbb66497a)
- FDA Inspection 956581 - 2015-12-18
- FDA Inspection 739038 - 2011-07-01

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/christopher-w-buser/6a11d2e7-dcfa-4542-ba81-b4c6b244ef04)

Company: https://www.keypedia.com/companies/curium-netherlands-bv/bf229870-ff31-4a25-ac32-752b1713a6fa

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