# Norfolk Medical Products, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/norfolk-medical-products-inc/a2db596b-8351-4825-84cf-ed707065318d

> Inspection records and compliance data for Norfolk Medical Products, Inc. in Skokie, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Norfolk Medical Products, Inc.
- FEI Number: 1450392
- City: Skokie
- State: Illinois
- Country Name: United States
- Address Line 1: 7350 Ridgeway Ave
- Zip Code: 60076

## Related Documents

- [FDA Inspection 1257901 - Norfolk Medical Products, Inc. - 2024-12-18](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/428d660a-fe7b-41ab-8eba-3a1d1a7b7d6d) — source: FDA, date: December 18, 2024
- [FDA Inspection 1257901 - Norfolk Medical Products, Inc. - 2024-12-18](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/cb028e71-b574-4c83-abd1-e1c7a15376e6) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2024
- [FDA Inspection 1257901 - Norfolk Medical Products, Inc. - 2024-12-18](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/aa348279-5aa8-4022-a61c-492369275cc7) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2024
- [483 - Norfolk Medical Products, Inc. - 2022-07-26](https://www.keypedia.com/records/483/norfolk-medical-products-inc/f8021711-cd6a-4725-84a7-e01ded32cd39) — source: FDA, date: July 26, 2022
- [FDA Inspection 1175430 - Norfolk Medical Products, Inc. - 2022-07-26](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/c96d4fc5-dcdd-4aa0-aad2-c263711e0af0) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2022
- [FDA Inspection 1175430 - Norfolk Medical Products, Inc. - 2022-07-26](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/df8482b8-e68c-4815-85a0-ee11580b3def) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 26, 2022
- [FDA Inspection 1071013 - Norfolk Medical Products, Inc. - 2018-11-02](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/f70938c8-f091-4016-ba24-5eec3f51d1e8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2018
- [FDA Inspection 914263 - Norfolk Medical Products, Inc. - 2015-02-11](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/a7182e85-300b-48e8-82ef-6ec942919f94) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2015
- [FDA Inspection 914263 - Norfolk Medical Products, Inc. - 2015-02-11](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/f7eca577-90ea-459a-92b5-9f3cd47b8666) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2015
- [FDA Inspection 644310 - Norfolk Medical Products, Inc. - 2010-02-04](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/7e6d86e9-14ec-4853-8e2b-3dbdba1f7930) — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2010
- [FDA Inspection 644310 - Norfolk Medical Products, Inc. - 2010-02-04](https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/ea7adf05-55c4-4eb0-b980-ca32c8c7bd83) — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2010

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