# Alcor Scientific, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/alcor-scientific-inc/10e4888b-8d60-4e1c-92f0-93f2fe504b47

> Inspection records and compliance data for Alcor Scientific, Inc. in Smithfield, Rhode Island. Access full analysis and detailed observations.

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## Details

- Name: Alcor Scientific, Inc.
- FEI Number: 3003855297
- City: Smithfield
- State: Rhode Island
- Country Name: United States
- Address Line 1: 20 Thurber Blvd
- Zip Code: 02917

## Related Documents

- [FDA Inspection 1074839 - Alcor Scientific, Inc. - 2018-12-18](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/9a047829-9291-4065-bd0f-dee29a2f2ac0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2018
- [FDA Inspection 1074839 - Alcor Scientific, Inc. - 2018-12-18](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/4575a1ea-8113-4e0c-834e-86768cc4ded2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2018
- [FDA Inspection 782014 - Alcor Scientific, Inc. - 2012-05-09](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/5f6eede0-e607-49ee-9eda-a090e0afacf8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2012
- [FDA Inspection 782014 - Alcor Scientific, Inc. - 2012-05-09](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/2ff4424e-e454-4149-b73b-29004830d826) — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2012
- [FDA Inspection 718263 - Alcor Scientific, Inc. - 2011-03-30](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/2c8ac348-071e-478b-99fc-fd8fad3da477) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2011
- [FDA Inspection 638618 - Alcor Scientific, Inc. - 2009-12-31](https://www.globalkeysolutions.net/records/fda_inspections/alcor-scientific-inc/9c48e080-e1d7-42d2-a93c-6addcc818bb9) — classification: Official Action Indicated (OAI), source: FDA, date: December 31, 2009

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