# FDA Inspection 1288064 - DS REP B.V. - October 17, 2025

Source: https://www.keypedia.com/records/fda_inspections/ds-rep-bv/58b2a494-b0b5-4aaf-9272-7df8c2c63def
Source feed: FDA_Inspections

> FDA Inspection 1288064 for DS REP B.V. on October 17, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288064
- Company Name: DS REP B.V.
- Inspection Date: 2025-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1288064 - 2025-10-17](https://www.keypedia.com/records/fda_inspections/ds-rep-bv/b329a9f1-c6b7-435a-b0fc-289a85c11547)
- [FDA Inspection 1288064 - 2025-10-17](https://www.keypedia.com/records/fda_inspections/ds-rep-bv/f1b8cc60-11c5-4a78-93ba-ceff4f6f388e)
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- [FDA Inspection 1046784 - 2018-03-23](https://www.keypedia.com/records/fda_inspections/ds-rep-bv/4a2e584d-fbb1-4841-a099-05226caa7652)

Company: https://www.keypedia.com/companies/ds-rep-bv/72eac62e-7ba1-46ff-8139-383dcd7cd6e4

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