# FDA Inspection 1179502 - ITG Int. - August 31, 2022

Source: https://www.keypedia.com/records/fda_inspections/itg-int/a829f6f2-0b7c-4ddf-bb39-5bb5f2d925a4
Source feed: FDA_Inspections

> FDA Inspection 1179502 for ITG Int. on August 31, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179502
- Company Name: ITG Int.
- Inspection Date: 2022-08-31
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179502 - 2022-08-31](https://www.keypedia.com/records/fda_inspections/itg-int/edacf273-f37d-4eef-b9fb-1a29e69988ed)
- [FDA Inspection 1031096 - 2017-10-20](https://www.keypedia.com/records/fda_inspections/itg-int/1cd2811f-f8ea-4524-a12e-6a1ae9876eec)
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Company: https://www.keypedia.com/companies/itg-int/b5e1823b-d6aa-4c14-a247-d81984ae8195

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