# CordenPharma Brussels SA, Brussels, Belgium – FDA Inspections

Source: https://www.keypedia.com/companies/cordenpharma-brussels-sa/2f748258-ca7e-4e98-ba82-824fe80fdd75

> Inspection records and compliance data for CordenPharma Brussels SA in Brussels. 5 FDA inspections on record, 1 Form 483, last inspected January 31, 2020.

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## Details

- Name: CordenPharma Brussels SA
- FEI Number: 3002807851
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Rue de Ransbeek 310
- City: Brussels
- Country Name: Belgium
- Address: Rue de Ransbeek 310, Brussels, Belgium
- Country: Belgium

## Related Documents

- FDA Inspection 1167305 - CordenPharma Brussels SA - 2020-01-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 31, 2020
- [FDA Inspection 1005031 - CordenPharma Brussels SA - 2017-02-03](https://www.keypedia.com/records/fda_inspections/cordenpharma-brussels-sa/440f5678-e355-4991-98c0-7db346dc57b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2017
- FDA Inspection 917907 - CordenPharma Brussels SA - 2015-02-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 27, 2015
- FDA Inspection 819585 - CordenPharma Brussels SA - 2013-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- FDA Inspection 584458 - CordenPharma Brussels SA - 2009-04-02 — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2009

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