# Product Design and Development Corp., Ellisville, MO – FDA Inspections

Source: https://www.keypedia.com/companies/product-design-and-development-corp/7159aa80-c032-42e7-a2f8-4e907c4bfe0c

> Inspection records and compliance data for Product Design and Development Corp. in Ellisville, Missouri. 4 FDA inspections on record, 2 Form 483s, last inspected January 24, 2025.

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## Details

- Name: Product Design and Development Corp.
- FEI Number: 3008146975
- Address Line 1: 16337 Westwoods Business Park
- City: Ellisville
- State: Missouri
- Zip Code: 63021
- Country Name: United States
- Address: 16337 Westwoods Business Park, Ellisville, Missouri 63021, United States
- Country: United States

## Related Documents

- [483 - Product Design and Development Corp. - 2025-01-24](https://www.keypedia.com/records/483/product-design-and-development-corp/91276afc-e93f-4bde-8f47-844795054c95) — source: FDA, date: January 24, 2025
- FDA Inspection 1259012 - Product Design and Development Corp. - 2025-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2025
- [FDA Inspection 1259012 - Product Design and Development Corp. - 2025-01-24](https://www.keypedia.com/records/fda_inspections/product-design-and-development-corp/833f8958-d09a-4d52-a6dc-b82c47cdd192) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2025
- FDA Inspection 1259012 - Product Design and Development Corp. - 2025-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2025
- FDA Inspection 1259012 - Product Design and Development Corp. - 2025-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2025
- [483 - Product Design and Development Corp. - 2022-03-17](https://www.keypedia.com/records/483/product-design-and-development-corp/ef1bd49d-a601-4d00-8f6e-3b0c8be37e42) — source: FDA, date: March 17, 2022
- FDA Inspection 1165801 - Product Design and Development Corp. - 2022-03-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2022
- FDA Inspection 1165801 - Product Design and Development Corp. - 2022-03-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2022
- FDA Inspection 1007077 - Product Design and Development Corp. - 2017-03-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2017
- [FDA Inspection 1007077 - Product Design and Development Corp. - 2017-03-30](https://www.keypedia.com/records/fda_inspections/product-design-and-development-corp/bba95350-e8e9-43dd-a295-c830d7439afe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2017
- [FDA Inspection 705631 - Product Design and Development Corp. - 2011-01-18](https://www.keypedia.com/records/fda_inspections/product-design-and-development-corp/a72c35be-b495-4d6a-b249-8f64cb1fe286) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 18, 2011

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