# DiaPharma Group Inc, West Chester, OH – FDA Inspections

Source: https://www.keypedia.com/companies/diapharma-group-inc/1778c90b-7a40-4a54-b058-a6f4ec274e7a

> Inspection records and compliance data for DiaPharma Group Inc in West Chester, Ohio. 5 FDA inspections on record (1 OAI), last inspected February 25, 2026.

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## Details

- Name: DiaPharma Group Inc
- FEI Number: 3000719074
- Address Line 1: 8948 Beckett Rd
- City: West Chester
- State: Ohio
- Zip Code: 45069
- Country Name: United States
- Address: 8948 Beckett Rd, West Chester, Ohio 45069, United States
- Country: United States

## Related Documents

- FDA Inspection 1306606 - DiaPharma Group Inc - 2026-02-25 — source: FDA, date: February 25, 2026
- FDA Inspection 1306606 - DiaPharma Group Inc - 2026-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2026
- FDA Inspection 1306606 - DiaPharma Group Inc - 2026-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2026
- [483 - DiaPharma Group Inc - 2022-04-29](https://www.keypedia.com/records/483/diapharma-group-inc/f39982cd-9155-433c-b756-f215adf693ec) — source: FDA, date: April 29, 2022
- [FDA Inspection 1171225 - DiaPharma Group Inc - 2022-04-29](https://www.keypedia.com/records/fda_inspections/diapharma-group-inc/b493f4de-ab73-489d-acc0-f6ce6e28fda6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2022
- FDA Inspection 940414 - DiaPharma Group Inc - 2015-08-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2015
- FDA Inspection 940414 - DiaPharma Group Inc - 2015-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2015
- FDA Inspection 749173 - DiaPharma Group Inc - 2011-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2011
- [FDA Inspection 712065 - DiaPharma Group Inc - 2011-03-08](https://www.keypedia.com/records/fda_inspections/diapharma-group-inc/79edb58b-f83d-409f-90da-800a7af2be94) — classification: Official Action Indicated (OAI), source: FDA, date: March 8, 2011

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