# FDA Inspection 1259012 - Product Design and Development Corp. - January 24, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/product-design-and-development-corp/da9ad288-7b36-43fb-89b9-a09da47286ff
Source feed: FDA_Inspections

> FDA Inspection 1259012 for Product Design and Development Corp. on January 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259012
- Company Name: Product Design and Development Corp.
- Inspection Date: 2025-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259012 - 2025-01-24](https://www.globalkeysolutions.net/records/fda_inspections/product-design-and-development-corp/833f8958-d09a-4d52-a6dc-b82c47cdd192)
- [FDA Inspection 1259012 - 2025-01-24](https://www.globalkeysolutions.net/records/fda_inspections/product-design-and-development-corp/4bd4e752-75bd-4209-94a3-d04f1f144f10)
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Company: https://www.globalkeysolutions.net/companies/product-design-and-development-corp/7159aa80-c032-42e7-a2f8-4e907c4bfe0c

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7