# Swedish Orphan Biovitrum AB (Publ), Stockholm, Sweden – FDA Inspections

Source: https://www.keypedia.com/companies/swedish-orphan-biovitrum-ab-publ/ce015a15-5a97-47dd-9e01-2bd5eb4b40f7

> Inspection records and compliance data for Swedish Orphan Biovitrum AB (Publ) in Stockholm. 7 FDA inspections on record, 1 Form 483, last inspected August 29, 2019.

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## Details

- Name: Swedish Orphan Biovitrum AB (Publ)
- FEI Number: 3003455777
- Address Line 1: Strandbergsgatan 49
- City: Stockholm
- Country Name: Sweden
- Address: Strandbergsgatan 49, Stockholm, Sweden
- Country: Sweden

## Related Documents

- FDA Inspection 1105180 - Swedish Orphan Biovitrum AB (Publ) - 2019-08-29 — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2019
- [FDA Inspection 1050664 - Swedish Orphan Biovitrum AB (Publ) - 2018-05-04](https://www.keypedia.com/records/fda_inspections/swedish-orphan-biovitrum-ab-publ/fedd8529-51b4-48a4-a3ce-9099fcb8a7d3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2018
- FDA Inspection 965894 - Swedish Orphan Biovitrum AB (Publ) - 2016-03-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 22, 2016
- FDA Inspection 886772 - Swedish Orphan Biovitrum AB (Publ) - 2014-05-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2014
- FDA Inspection 822730 - Swedish Orphan Biovitrum AB (Publ) - 2013-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2013
- FDA Inspection 725457 - Swedish Orphan Biovitrum AB (Publ) - 2011-01-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2011
- FDA Inspection 725457 - Swedish Orphan Biovitrum AB (Publ) - 2011-01-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2011
- FDA Inspection 569950 - Swedish Orphan Biovitrum AB (Publ) - 2009-01-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 20, 2009

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