# Regeneron Pharmaceuticals Inc - Inspection Records

Source: https://www.keypedia.com/companies/regeneron-pharmaceuticals-inc/fbb2cea0-65e4-4da9-9c5f-eea90c33a84f

> Inspection records and compliance data for Regeneron Pharmaceuticals Inc in Tarrytown, New York. Access full analysis and detailed observations.

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## Details

- Name: Regeneron Pharmaceuticals Inc
- FEI Number: 1000521995
- City: Tarrytown
- State: New York
- Country Name: United States
- Address Line 1: 777 Old Saw Mill River Rd
- Zip Code: 10591

## Related Documents

- [FDA Inspection 1292476 - Regeneron Pharmaceuticals Inc - 2025-12-10](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/f32684d9-704d-40e5-96c3-6e4ae998055e) — source: FDA, date: December 10, 2025
- [FDA Inspection 1292476 - Regeneron Pharmaceuticals Inc - 2025-12-10](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/73a221d2-f485-4743-87ce-67ffd7532740) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2025
- [FDA Inspection 1232732 - Regeneron Pharmaceuticals Inc - 2024-05-01](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/b8b32e56-a0a8-49bd-8b60-00af143c362b) — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2024
- [FDA Inspection 1228712 - Regeneron Pharmaceuticals Inc - 2024-01-19](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/a36b4ea2-1103-4135-b2fe-510e643f7ea4) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2024
- [FDA Inspection 1156180 - Regeneron Pharmaceuticals Inc - 2021-10-15](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/e66f35fc-9862-4dea-a281-af38a78097ea) — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2021
- [FDA Inspection 1134447 - Regeneron Pharmaceuticals Inc - 2020-12-21](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/1b3b73ae-ab43-4de0-8c1c-5143a3592271) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2020
- [FDA Inspection 1117465 - Regeneron Pharmaceuticals Inc - 2020-01-17](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/2335ccb2-402f-4d29-9b38-9f0f2be793f0) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2020
- [FDA Inspection 1068761 - Regeneron Pharmaceuticals Inc - 2018-09-17](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/c7651fd9-26b7-481f-8b88-a8d9649f18dd) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2018
- [FDA Inspection 1067515 - Regeneron Pharmaceuticals Inc - 2018-08-10](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/81077b2a-31db-42ee-b626-9f473d05f141) — classification: No Action Indicated (NAI), source: FDA, date: August 10, 2018
- [FDA Inspection 1057304 - Regeneron Pharmaceuticals Inc - 2018-06-18](https://www.keypedia.com/records/fda_inspections/regeneron-pharmaceuticals-inc/15c72eac-e133-48be-838a-4cd79f184ead) — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2018

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