# Grupo Pozuelo & PRO GPP, S.A. - Inspection Records

Source: https://www.keypedia.com/companies/grupo-pozuelo-pro-gpp-sa/d4c96d80-2f57-45c8-b25e-30babffa5385

> Inspection records and compliance data for Grupo Pozuelo & PRO GPP, S.A. in Ciudad Colon, None. Access full analysis and detailed observations.

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## Details

- Name: Grupo Pozuelo & PRO GPP, S.A.
- FEI Number: 3004286612
- City: Ciudad Colon
- State: None
- Country Name: Costa Rica
- Address Line 1: Calle Las Carreras
- Zip Code: None

## Related Documents

- [FDA Inspection 1209289 - Grupo Pozuelo & PRO GPP, S.A. - 2023-06-29](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/321aed3b-dccd-4893-b7c0-506b005f81ae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2023
- [FDA Inspection 1209289 - Grupo Pozuelo & PRO GPP, S.A. - 2023-06-29](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/84eb54eb-cbf8-4c74-8ff8-2f66868bec68) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2023
- [FDA Inspection 1010438 - Grupo Pozuelo & PRO GPP, S.A. - 2017-04-19](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/f60bf846-db63-4cb3-9dfe-353be2027608) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2017
- [FDA Inspection 1010438 - Grupo Pozuelo & PRO GPP, S.A. - 2017-04-19](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/ef83aef6-b4f7-461f-b781-3cd23f234b8b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2017
- [FDA Inspection 807251 - Grupo Pozuelo & PRO GPP, S.A. - 2012-11-16](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/23c109ad-20e9-41eb-90e5-ecc272884c9c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2012
- [FDA Inspection 807251 - Grupo Pozuelo & PRO GPP, S.A. - 2012-11-16](https://www.keypedia.com/records/fda_inspections/grupo-pozuelo-pro-gpp-sa/718f5fa6-d0c0-49ba-a3e4-e625322fb781) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2012

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