# Merck Serono SA (Vevey) - Inspection Records

Source: https://www.keypedia.com/companies/merck-serono-sa-vevey/e86df39a-6cb6-4ab2-a811-47c8369ba270

> Inspection records and compliance data for Merck Serono SA (Vevey) in Corsier-Sur-Vevey, None. Access full analysis and detailed observations.

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## Details

- Name: Merck Serono SA (Vevey)
- FEI Number: 3003131678
- City: Corsier-Sur-Vevey
- State: None
- Country Name: Switzerland
- Address Line 1: Route De Fenil Z.I.B
- Zip Code: None

## Related Documents

- [483 - Merck Serono SA (Vevey) - 2023-04-06](https://www.keypedia.com/records/483/merck-serono-sa-vevey/5c270aad-9199-45d5-9162-240223e421a4) — source: FDA, date: April 6, 2023
- [483 - Merck Serono SA (Vevey) - 2023-04-06](https://www.keypedia.com/records/483/merck-serono-sa-vevey/c34c627c-a097-4956-b8f6-66f8d567d2fe) — source: FDA, date: April 6, 2023
- [FDA Inspection 1204345 - Merck Serono SA (Vevey) - 2023-04-06](https://www.keypedia.com/records/fda_inspections/merck-serono-sa-vevey/dc32ca15-1a57-481c-92e3-5297366fb5a5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 6, 2023
- [FDA Inspection 1053823 - Merck Serono SA (Vevey) - 2018-04-30](https://www.keypedia.com/records/fda_inspections/merck-serono-sa-vevey/8ccd1fc4-b807-4132-b296-0ba2a0591f99) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2018
- [FDA Inspection 964102 - Merck Serono SA (Vevey) - 2016-02-05](https://www.keypedia.com/records/fda_inspections/merck-serono-sa-vevey/99c8aa74-4800-4e49-825b-5db788107c32) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 5, 2016
- [FDA Inspection 811116 - Merck Serono SA (Vevey) - 2012-11-06](https://www.keypedia.com/records/fda_inspections/merck-serono-sa-vevey/16922ac4-3180-496f-a444-6a00f5952477) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2012
- [FDA Inspection 732618 - Merck Serono SA (Vevey) - 2011-06-09](https://www.keypedia.com/records/fda_inspections/merck-serono-sa-vevey/94560388-a1bb-4c0e-96eb-e4d514dddaf3) — classification: Official Action Indicated (OAI), source: FDA, date: June 9, 2011

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