# Megadyne Medical Products, Inc., Blue Ash, OH – FDA Inspections

Source: https://www.keypedia.com/companies/megadyne-medical-products-inc/1804c069-f60b-4da8-8b6c-43e0de13c11b

> Inspection records and compliance data for Megadyne Medical Products, Inc. in Blue Ash, Ohio. 5 FDA inspections on record, last inspected November 22, 2024.

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## Details

- Name: Megadyne Medical Products, Inc.
- FEI Number: 1721194
- Address Line 1: 4545 Creek Rd
- City: Blue Ash
- State: Ohio
- Zip Code: 45242
- Country Name: United States
- Address: 4545 Creek Rd, Blue Ash, Ohio 45242, United States
- Country: United States

## Related Documents

- FDA Inspection 1256322 - Megadyne Medical Products, Inc. - 2024-11-22 — source: FDA, date: November 22, 2024
- FDA Inspection 1256322 - Megadyne Medical Products, Inc. - 2024-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2024
- FDA Inspection 1256322 - Megadyne Medical Products, Inc. - 2024-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2024
- FDA Inspection 1208218 - Megadyne Medical Products, Inc. - 2023-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2023
- FDA Inspection 1208218 - Megadyne Medical Products, Inc. - 2023-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2023
- FDA Inspection 955782 - Megadyne Medical Products, Inc. - 2015-12-11 — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2015
- FDA Inspection 955782 - Megadyne Medical Products, Inc. - 2015-12-11 — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2015
- FDA Inspection 809350 - Megadyne Medical Products, Inc. - 2012-12-06 — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2012
- FDA Inspection 809350 - Megadyne Medical Products, Inc. - 2012-12-06 — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2012
- FDA Inspection 632644 - Megadyne Medical Products, Inc. - 2009-12-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 10, 2009

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