# DS REP B.V. – FDA Inspection, Mar 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/ds-rep-bv/4a2e584d-fbb1-4841-a099-05226caa7652
Source feed: FDA_Inspections

> FDA inspection 1046784 of DS REP B.V., March 23, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046784
- Company Name: DS REP B.V.
- Inspection Date: 2018-03-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- [FDA Inspection 821728 - 2013-03-06](https://www.keypedia.com/records/fda_inspections/ds-rep-bv/4f95d7a2-180d-488d-9a04-798955c61d3e)
- FDA Inspection 652360 - 2010-03-18

## Related Officers

- [Investigator](https://www.keypedia.com/people/nydia-e-colon/c5137ded-6ae7-4855-b5b3-113bd851e1c3)

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