# Repro-Med Systems, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/repro-med-systems-inc/33ca025a-ec91-4b0c-ae99-ac661170de7e

> Inspection records and compliance data for Repro-Med Systems, Inc. in Chester, New York. Access full analysis and detailed observations.

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## Details

- Name: Repro-Med Systems, Inc.
- FEI Number: 1318360
- City: Chester
- State: New York
- Country Name: United States
- Address Line 1: 24 Carpenter Rd
- Zip Code: 10918
- Facility Type: Medical Device Manufacturer

## Related Documents

- [483 - Repro-Med Systems, Inc. - 2017-10-19](https://www.keypedia.com/records/483/repro-med-systems-inc/75802b90-2603-4d03-b633-aa4ea5a69b03) — source: FDA, date: October 19, 2017
- [FDA Inspection 1029627 - Repro-Med Systems, Inc. - 2017-10-19](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/b278a98f-1b2d-4816-a28b-03b7d9064473) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2017
- [FDA Inspection 1029627 - Repro-Med Systems, Inc. - 2017-10-19](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/b794adc6-ca44-4acb-9efa-3ba57d3934bf) — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2017
- [483 - Repro-Med Systems, Inc. - 2016-12-16](https://www.keypedia.com/records/483/repro-med-systems-inc/6594af00-3003-4ed8-889d-5d5fd326cd0c) — source: FDA, date: December 16, 2016
- [FDA Inspection 996093 - Repro-Med Systems, Inc. - 2016-12-16](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/0ac00916-4fe9-4b11-bf62-d3a8ef4a40e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2016
- [FDA Inspection 996093 - Repro-Med Systems, Inc. - 2016-12-16](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/ca0b7afe-57e2-43ac-8005-9591400d9a99) — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2016
- [FDA Inspection 929452 - Repro-Med Systems, Inc. - 2015-06-23](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/a302eb26-b1cb-42c4-a720-f7bac8985b2d) — classification: Official Action Indicated (OAI), source: FDA, date: June 23, 2015
- [FDA Inspection 929452 - Repro-Med Systems, Inc. - 2015-06-23](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/f30e24d8-0d40-417a-8e4c-2fdfc24950db) — classification: Official Action Indicated (OAI), source: FDA, date: June 23, 2015
- [FDA Inspection 793650 - Repro-Med Systems, Inc. - 2012-07-20](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/f86f29ac-89ca-4802-8792-8fb741afb9a1) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2012
- [FDA Inspection 793650 - Repro-Med Systems, Inc. - 2012-07-20](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/c6566f74-530c-40f0-8a16-964d0bf4a767) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2012
- [FDA Inspection 683171 - Repro-Med Systems, Inc. - 2010-09-21](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/5e26b65c-d1b0-41b4-81e0-afabfd491de1) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2010
- [FDA Inspection 683171 - Repro-Med Systems, Inc. - 2010-09-21](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/b73c2e57-ed2a-401a-a30d-260bdc0a6a40) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2010

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## Related Officers

- [Scott R. Izyk](https://www.keypedia.com/people/scott-r-izyk/ce6f1f5a-10ed-4c83-a3d4-7e3692b57a51)
- [investigator](https://www.keypedia.com/people/li-lu/fa120f19-beac-4d2d-8059-339a93911b85)