# FDA Inspection 1230619 - Imedia NY Inc - October 23, 2024

Source: https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/9cdd8e89-fd6c-4bd3-aa17-8315ef9ea763
Source feed: FDA_Inspections

> FDA Inspection 1230619 for Imedia NY Inc on October 23, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1230619
- Company Name: Imedia NY Inc
- Inspection Date: 2024-10-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1230619 - 2024-10-23](https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/1a517de7-1095-4c82-96dc-2ac8d92dca38)
- [FDA Inspection 1230619 - 2024-10-23](https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/f2a6421d-8f46-48a5-9b12-bbf231615bc8)
- [FDA Inspection 1230619 - 2024-10-23](https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/9ae0e8d9-101d-4167-8087-92fb48ee6428)
- [FDA Inspection 1122424 - 2020-01-16](https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/5c4b4725-0c55-4170-9675-b9f125de40d9)
- [FDA Inspection 1122424 - 2020-01-16](https://www.keypedia.com/records/fda_inspections/imedia-ny-inc/852b3062-e98f-4a99-a0b1-e6b9e9874a16)

Company: https://www.keypedia.com/companies/imedia-ny-inc/7595ea20-ae65-4ef9-b329-005add214487

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