# FDA Inspection 1179719 - Numotech Inc - September 09, 2022

Source: https://www.keypedia.com/records/fda_inspections/numotech-inc/22d1460d-252b-4ee4-acc8-e8b5a745e0fe
Source feed: FDA_Inspections

> FDA Inspection 1179719 for Numotech Inc on September 09, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179719
- Company Name: Numotech Inc
- Inspection Date: 2022-09-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179719 - 2022-09-09](https://www.keypedia.com/records/fda_inspections/numotech-inc/1b6dc185-6c93-47d4-9e74-4a47917f0384)
- [FDA Inspection 1004210 - 2017-03-06](https://www.keypedia.com/records/fda_inspections/numotech-inc/a026d281-0332-4a89-82dd-f0350ec1494c)
- [FDA Inspection 824920 - 2013-04-01](https://www.keypedia.com/records/fda_inspections/numotech-inc/09ba75e9-4dc4-4a3d-82aa-d94141e3cfd3)
- [FDA Inspection 824920 - 2013-04-01](https://www.keypedia.com/records/fda_inspections/numotech-inc/10d18c0c-182d-4b81-b6da-f754adb5eaf9)
- [FDA Inspection 682676 - 2010-09-20](https://www.keypedia.com/records/fda_inspections/numotech-inc/0894825e-502b-4428-a627-c3eb8df682a5)

Company: https://www.keypedia.com/companies/numotech-inc/2d28948c-8129-4a6d-86ab-b10ea2e380f4

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