# MP Biomedicals Diagnostics Division, Solon, OH – FDA Inspections

Source: https://www.keypedia.com/companies/mp-biomedicals-diagnostics-division/9f3cc4ba-9268-40d8-a76e-8f7f44361991

> Inspection records and compliance data for MP Biomedicals Diagnostics Division in Solon, Ohio. 4 FDA inspections on record (1 OAI), 2 Form 483s, last inspected March 31, 2026.

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## Details

- Name: MP Biomedicals Diagnostics Division
- FEI Number: 2419955
- Address Line 1: 29525 Fountain Pkwy
- City: Solon
- State: Ohio
- Zip Code: 44139
- Country Name: United States
- Address: 29525 Fountain Pkwy, Solon, Ohio 44139, United States
- Country: United States

## Related Documents

- [FDA Inspection 1310200 - MP Biomedicals Diagnostics Division - 2026-03-31](https://www.keypedia.com/records/fda_inspections/mp-biomedicals-diagnostics-division/2cc0bce1-369e-447c-a594-80fd59ea225f) — source: FDA, date: March 31, 2026
- [FDA Inspection 1034831 - MP Biomedicals Diagnostics Division - 2017-12-13](https://www.keypedia.com/records/fda_inspections/mp-biomedicals-diagnostics-division/5ce56b9a-3b6c-47e1-be63-3f264d38cbfd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2017
- FDA Inspection 1034831 - MP Biomedicals Diagnostics Division - 2017-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2017
- FDA Inspection 760696 - MP Biomedicals Diagnostics Division - 2011-12-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 15, 2011
- FDA Inspection 760696 - MP Biomedicals Diagnostics Division - 2011-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2011
- [FDA Inspection 657363 - MP Biomedicals Diagnostics Division - 2010-04-22](https://www.keypedia.com/records/fda_inspections/mp-biomedicals-diagnostics-division/c026c396-c909-43b7-af65-c26fb900f338) — classification: Official Action Indicated (OAI), source: FDA, date: April 22, 2010
- FDA Inspection 657363 - MP Biomedicals Diagnostics Division - 2010-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2010

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