# Edward M. Kerwin, M.D - Inspection Records

Source: https://www.globalkeysolutions.net/companies/edward-m-kerwin-md/aed94e36-e6bd-4215-8c9d-916634ac93e8

> Inspection records and compliance data for Edward M. Kerwin, M.D in Medford, Oregon. Access full analysis and detailed observations.

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## Details

- Name: Edward M. Kerwin, M.D
- FEI Number: 3003591924
- City: Medford
- State: Oregon
- Country Name: United States
- Address Line 1: 3860 Crater Lake Ave Ste B
- Zip Code: 97504
- Business Operations: CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY

## Related Documents

- [FDA Inspection 1133259 - Edward M. Kerwin, M.D - 2020-11-13](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/04f5737a-18ee-425e-9482-6c10cddb00da) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2020
- [FDA Inspection 1133259 - Edward M. Kerwin, M.D - 2020-11-13](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/4469a0ed-2639-4f6f-856d-6daa72f4b05e) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2020
- [FDA Inspection 1041339 - Edward M. Kerwin, M.D - 2018-01-19](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/faf12336-0438-45b0-a35e-9cabcf7b1f76) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2018
- [FDA Inspection 836858 - Edward M. Kerwin, M.D - 2013-06-20](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/ef419ad0-7fe3-4d1f-a1d7-cec47634edc9) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2013
- [FDA Inspection 830397 - Edward M. Kerwin, M.D - 2012-10-17](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/0b501813-b836-4b00-9fb1-295a5c5aac0c) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2012
- [FDA Inspection 614760 - Edward M. Kerwin, M.D - 2009-09-18](https://www.globalkeysolutions.net/records/fda_inspections/edward-m-kerwin-md/57a77871-95b7-4e1f-a87e-94d9f03fcc04) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2009

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