# FDA Inspection 948392 - Durtech System Corp. - October 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/durtech-system-corp/31b52a19-ee80-4784-9348-813eaf0a04b0
Source feed: FDA_Inspections

> FDA Inspection 948392 for Durtech System Corp. on October 21, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 948392
- Company Name: Durtech System Corp.
- Inspection Date: 2015-10-21
- 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 948392 - 2015-10-21](https://www.keypedia.com/records/fda_inspections/durtech-system-corp/833f3641-1610-495c-9084-fff81e027a5c)

Company: https://www.keypedia.com/companies/durtech-system-corp/b2cae803-c814-4753-8872-38e639da3451

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