# Fresenius Kabi AB, Uppsala, Sweden – FDA Inspections

Source: https://www.keypedia.com/companies/fresenius-kabi-ab/95acd39b-72be-48a9-aa55-38713a33c8cc

> Inspection records and compliance data for Fresenius Kabi AB in Uppsala. 8 FDA inspections on record, 1 Form 483, last inspected April 21, 2023.

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## Details

- Name: Fresenius Kabi AB
- FEI Number: 3002631703
- Business Operations: API MANUFACTURE, FDF MANUFACTURE
- Address Line 1: Rapsgatan 7
- City: Uppsala
- Country Name: Sweden
- Address: Rapsgatan 7, Uppsala, Sweden
- Country: Sweden

## Related Documents

- FDA Inspection 1238177 - Fresenius Kabi AB - 2023-04-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2023
- FDA Inspection 1238177 - Fresenius Kabi AB - 2023-04-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2023
- FDA Inspection 1155467 - Fresenius Kabi AB - 2020-10-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2020
- [FDA Inspection 1099421 - Fresenius Kabi AB - 2018-10-16](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/601d4a6e-431f-4514-affd-3f8945416a3c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 16, 2018
- [FDA Inspection 1005000 - Fresenius Kabi AB - 2017-02-07](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/5335bdf2-a6c2-4615-9a8d-e8c7eb43064f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2017
- FDA Inspection 1005000 - Fresenius Kabi AB - 2017-02-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2017
- FDA Inspection 925969 - Fresenius Kabi AB - 2015-03-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2015
- FDA Inspection 876533 - Fresenius Kabi AB - 2014-04-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2014
- FDA Inspection 876533 - Fresenius Kabi AB - 2014-04-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2014
- FDA Inspection 802513 - Fresenius Kabi AB - 2012-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2012

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