# DS REP B.V. – FDA Inspection, Mar 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/ds-rep-bv/4f95d7a2-180d-488d-9a04-798955c61d3e
Source feed: FDA_Inspections

> FDA inspection 821728 of DS REP B.V., March 06, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 821728
- Company Name: DS REP B.V.
- Inspection Date: 2013-03-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1288064 - 2025-10-17
- FDA Inspection 1173360 - 2022-06-16
- [FDA Inspection 1046784 - 2018-03-23](https://www.keypedia.com/records/fda_inspections/ds-rep-bv/4a2e584d-fbb1-4841-a099-05226caa7652)
- FDA Inspection 652360 - 2010-03-18

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