# FDA Inspection 1020606 - Diotech Co. Ltd. - July 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/diotech-co-ltd/ab2d3efd-90e1-4619-a57c-720960047f5b
Source feed: FDA_Inspections

> FDA Inspection 1020606 for Diotech Co. Ltd. on July 28, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020606
- Company Name: Diotech Co. Ltd.
- Inspection Date: 2017-07-28
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020606 - 2017-07-28](https://www.keypedia.com/records/fda_inspections/diotech-co-ltd/598dc9fe-9d97-498c-af89-62a294f423f5)
- [FDA Inspection 1020606 - 2017-07-28](https://www.keypedia.com/records/fda_inspections/diotech-co-ltd/190069ac-9309-4ad8-9f0b-3b8fc7ddde45)

Company: https://www.keypedia.com/companies/diotech-co-ltd/4a5e0b21-ac21-4f32-9ef2-85dddc07098e

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