# Kem Medical Products Corp - Inspection Records

Source: https://www.keypedia.com/companies/kem-medical-products-corp/839eba3c-ce65-4e39-a7a5-7258eddea42a

> Inspection records and compliance data for Kem Medical Products Corp in Hauppauge, New York. Access full analysis and detailed observations.

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## Details

- Name: Kem Medical Products Corp
- FEI Number: 2432141
- City: Hauppauge
- State: New York
- Country Name: United States
- Address Line 1: 400 Oser Ave
- Zip Code: 11788

## Related Documents

- [483 - Kem Medical Products Corp - 2022-07-21](https://www.keypedia.com/records/483/kem-medical-products-corp/75775f7f-d4f9-47e5-b237-c4af74083468) — source: FDA, date: July 21, 2022
- [FDA Inspection 1175436 - Kem Medical Products Corp - 2022-07-21](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/1e0a4651-28fc-4161-a8bf-e8636800e1e9) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2022
- [FDA Inspection 1175436 - Kem Medical Products Corp - 2022-07-21](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/50793f7c-11b8-4d87-a61a-7778ec2b683c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2022
- [483 - Kem Medical Products Corp - 2020-01-15](https://www.keypedia.com/records/483/kem-medical-products-corp/d29db142-9f8a-4e62-8980-30c4628a49bc) — source: FDA, date: January 15, 2020
- [FDA Inspection 1115221 - Kem Medical Products Corp - 2020-01-15](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/7ee249a5-0713-4d27-b798-ecb7d1247089) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2020
- [FDA Inspection 1115221 - Kem Medical Products Corp - 2020-01-15](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/a27e28e9-6290-4f2c-b798-6b3e218a03ed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2020
- [FDA Inspection 1003651 - Kem Medical Products Corp - 2017-02-21](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/1f7f0e4f-a937-4ac5-8042-820f82f32197) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2017
- [FDA Inspection 791042 - Kem Medical Products Corp - 2012-07-10](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/277950a4-0bbf-43a6-ba7e-5bf968e5832c) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2012
- [FDA Inspection 791042 - Kem Medical Products Corp - 2012-07-10](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/3b432a46-8d45-4429-96b9-c784cd3104e3) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2012
- [FDA Inspection 623870 - Kem Medical Products Corp - 2009-10-27](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/19622308-fea7-4b95-bf14-6ef3e8e52cc1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2009
- [FDA Inspection 623870 - Kem Medical Products Corp - 2009-10-27](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/165ba505-13bc-4afa-9939-823eec7a350b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2009

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