# FDA Inspection 1249662 - Ideavillage Products Corp. - September 20, 2024

Source: https://www.keypedia.com/records/fda_inspections/ideavillage-products-corp/8d8f60c1-c7a3-4e34-a6b9-2451a3f1cd9a
Source feed: FDA_Inspections

> FDA Inspection 1249662 for Ideavillage Products Corp. on September 20, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1249662
- Company Name: Ideavillage Products Corp.
- Inspection Date: 2024-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New Jersey District Office

## Related Documents

- [FDA Inspection 1249662 - 2024-09-20](https://www.keypedia.com/records/fda_inspections/ideavillage-products-corp/e5cf3234-d3b7-463e-8476-70c86e52f58b)
- [FDA Inspection 1249662 - 2024-09-20](https://www.keypedia.com/records/fda_inspections/ideavillage-products-corp/cd53d49e-494d-4007-a579-3ec42ce5a73f)
- [FDA Inspection 1249662 - 2024-09-20](https://www.keypedia.com/records/fda_inspections/ideavillage-products-corp/29b981c1-8b08-4ae2-ba95-205b67d28f33)

Company: https://www.keypedia.com/companies/ideavillage-products-corp/fac9c87a-0b77-4af2-b11a-e6b3a357587c

Office: https://www.keypedia.com/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248