# GE Healthcare AS, Oslo, Norway – FDA Inspections

Source: https://www.keypedia.com/companies/ge-healthcare-as/1b18a0cb-bd39-4d75-b4c3-3540b36621e0

> Inspection records and compliance data for GE Healthcare AS in Oslo. 8 FDA inspections on record, 2 Form 483s, last inspected April 23, 2024.

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## Details

- Name: GE Healthcare AS
- FEI Number: 3002807779
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: Nycoveien 1
- City: Oslo
- Country Name: Norway
- Address: Nycoveien 1, Oslo, Norway
- Country: Norway

## Related Documents

- [FDA Inspection 1236691 - GE Healthcare AS - 2024-04-23](https://www.keypedia.com/records/fda_inspections/ge-healthcare-as/957ef9cd-70fb-4579-a3f4-24bfef801923) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 23, 2024
- [FDA Inspection 1100537 - GE Healthcare AS - 2019-08-27](https://www.keypedia.com/records/fda_inspections/ge-healthcare-as/c5b9616f-396b-4f7e-9d13-e2bb5eef80af) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 27, 2019
- [FDA Inspection 1037481 - GE Healthcare AS - 2017-11-10](https://www.keypedia.com/records/fda_inspections/ge-healthcare-as/765e0953-5fd7-4162-b821-5abb6cc37fef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2017
- FDA Inspection 959608 - GE Healthcare AS - 2016-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2016
- FDA Inspection 915526 - GE Healthcare AS - 2015-02-03 — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2015
- FDA Inspection 810910 - GE Healthcare AS - 2012-12-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2012
- [FDA Inspection 605126 - GE Healthcare AS - 2009-07-17](https://www.keypedia.com/records/fda_inspections/ge-healthcare-as/44ced21e-2e82-495e-94d2-4329554fa877) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2009
- FDA Inspection 601116 - GE Healthcare AS - 2009-07-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 9, 2009

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