# Debiopharm Research & Manufacturing S.A. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/debiopharm-research-manufacturing-sa/7b1cb6dd-011a-4539-abff-3459db2a38c8

> Inspection records and compliance data for Debiopharm Research & Manufacturing S.A. in Martigny, None. Access full analysis and detailed observations.

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## Details

- Name: Debiopharm Research & Manufacturing S.A.
- FEI Number: 3002806850
- City: Martigny
- State: None
- Country Name: Switzerland
- Address Line 1: Rue Du Levant 146
- Zip Code: None

## Related Documents

- [FDA Inspection 1199737 - Debiopharm Research & Manufacturing S.A. - 2023-03-14](https://www.globalkeysolutions.net/records/fda_inspections/debiopharm-research-manufacturing-sa/3acc693d-327d-45f5-a2d5-517adc842b32) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2023
- [FDA Inspection 1055095 - Debiopharm Research & Manufacturing S.A. - 2018-06-08](https://www.globalkeysolutions.net/records/fda_inspections/debiopharm-research-manufacturing-sa/5f99b556-01e7-4b3b-85dd-d6ccd1182835) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 8, 2018
- [FDA Inspection 987836 - Debiopharm Research & Manufacturing S.A. - 2016-09-07](https://www.globalkeysolutions.net/records/fda_inspections/debiopharm-research-manufacturing-sa/dd16bfdb-a4ac-46ac-94b0-c60f652e31d9) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2016
- [FDA Inspection 870230 - Debiopharm Research & Manufacturing S.A. - 2014-03-18](https://www.globalkeysolutions.net/records/fda_inspections/debiopharm-research-manufacturing-sa/44007650-8f20-4c76-bbfa-b1023d8116b7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2014
- [FDA Inspection 590703 - Debiopharm Research & Manufacturing S.A. - 2009-05-07](https://www.globalkeysolutions.net/records/fda_inspections/debiopharm-research-manufacturing-sa/6164c0bc-1ee4-4e27-b38f-960c5eb6d997) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2009

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