# Richard Wolf Medical Instruments Corp. - Inspection Records

Source: https://www.keypedia.com/companies/richard-wolf-medical-instruments-corp/35a87eec-34b1-4a3a-afc3-17b2c19ec98d

> Inspection records and compliance data for Richard Wolf Medical Instruments Corp. in Vernon Hills, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Richard Wolf Medical Instruments Corp.
- FEI Number: 1418479
- City: Vernon Hills
- State: Illinois
- Country Name: United States
- Address Line 1: 353 Corporate Woods Pkwy
- Zip Code: 60061

## Related Documents

- [FDA Inspection 1259420 - Richard Wolf Medical Instruments Corp. - 2025-01-13](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/34d3e511-abb4-48e2-86cd-b218a4986586) — source: FDA, date: January 13, 2025
- [FDA Inspection 1259420 - Richard Wolf Medical Instruments Corp. - 2025-01-13](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/a17c608a-4117-4542-9608-2f0a615d19ea) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2025
- [FDA Inspection 1259420 - Richard Wolf Medical Instruments Corp. - 2025-01-13](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/193b1ea2-fee0-4f6c-99b8-b7a0871d1219) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2025
- [FDA Inspection 1203639 - Richard Wolf Medical Instruments Corp. - 2023-04-19](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/8cdab96b-6b6f-47c2-a3ab-9c4f44dedf31) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2023
- [FDA Inspection 1203639 - Richard Wolf Medical Instruments Corp. - 2023-04-19](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/34aba4dc-41ca-49d3-b460-638ebed5565b) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2023
- [483 - Richard Wolf Medical Instruments Corp. - 2020-03-18](https://www.keypedia.com/records/483/richard-wolf-medical-instruments-corp/029b2b66-9035-456e-8ae2-49920e5337b7) — source: FDA, date: March 18, 2020
- [FDA Inspection 1121063 - Richard Wolf Medical Instruments Corp. - 2020-03-18](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/f363c4f7-04ff-4626-8368-ed3171967ad5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2020
- [FDA Inspection 1121063 - Richard Wolf Medical Instruments Corp. - 2020-03-18](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/e0f0a63e-47da-4450-807b-c895753fa35e) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2020
- [483 - Richard Wolf Medical Instruments Corp. - 2018-07-17](https://www.keypedia.com/records/483/richard-wolf-medical-instruments-corp/2cf4bf45-6623-43c2-83ac-f3db4eb2f6d2) — source: FDA, date: July 17, 2018
- [FDA Inspection 1059209 - Richard Wolf Medical Instruments Corp. - 2018-07-17](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/57b6c210-9e62-4cb9-8c78-040c96e4a37c) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2018
- [FDA Inspection 1059209 - Richard Wolf Medical Instruments Corp. - 2018-07-17](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/a62c1c04-3a3d-4eb6-8544-ab865e3c241c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2018
- [FDA Inspection 900890 - Richard Wolf Medical Instruments Corp. - 2014-10-10](https://www.keypedia.com/records/fda_inspections/richard-wolf-medical-instruments-corp/dd18b8bc-8323-4af2-9632-e986445506af) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 10, 2014
- [WARNING_LETTER - Richard Wolf Medical Instruments Corp. - 2013-05-08](https://www.keypedia.com/records/warning_letter/richard-wolf-medical-instruments-corp/eb9de329-a673-4c02-9a2c-914e750544ed) — source: FDA, date: May 8, 2013

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