# Towa Pharmaceutical Europe, S.L., Martorelles, Spain – FDA Inspections

Source: https://www.keypedia.com/companies/towa-pharmaceutical-europe-sl/731d0b47-ce02-4781-8582-7090b456c5fe

> Inspection records and compliance data for Towa Pharmaceutical Europe, S.L. in Martorelles. 6 FDA inspections on record, 1 Form 483, last inspected September 09, 2022.

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## Details

- Name: Towa Pharmaceutical Europe, S.L.
- FEI Number: 3003121577
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE
- Address Line 1: Calle De Sant Marti 75-97
- City: Martorelles
- Country Name: Spain
- Address: Calle De Sant Marti 75-97, Martorelles, Spain
- Country: Spain

## Related Documents

- [483 - Towa Pharmaceutical Europe, S.L. - 2022-09-09](https://www.keypedia.com/records/483/towa-pharmaceutical-europe-sl/2c556257-4901-4d7c-a4d1-2a060614bdc3) — source: FDA, date: September 9, 2022
- FDA Inspection 1180157 - Towa Pharmaceutical Europe, S.L. - 2022-09-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 9, 2022
- FDA Inspection 1100280 - Towa Pharmaceutical Europe, S.L. - 2019-01-18 — classification: No Action Indicated (NAI), source: FDA, date: January 18, 2019
- FDA Inspection 1018727 - Towa Pharmaceutical Europe, S.L. - 2017-03-31 — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2017
- [FDA Inspection 1018727 - Towa Pharmaceutical Europe, S.L. - 2017-03-31](https://www.keypedia.com/records/fda_inspections/towa-pharmaceutical-europe-sl/9948e85f-5b91-4a1e-998a-3e96ca2da81e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2017
- FDA Inspection 917425 - Towa Pharmaceutical Europe, S.L. - 2015-02-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 13, 2015
- FDA Inspection 835225 - Towa Pharmaceutical Europe, S.L. - 2013-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2013
- FDA Inspection 658164 - Towa Pharmaceutical Europe, S.L. - 2010-02-19 — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2010

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