# Diotech Co. Ltd. – FDA Inspection, Jul 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 of Diotech Co. Ltd., July 28, 2017. Classification: Official Action Indicated (OAI). 11 citations under 21 CFR parts 803, 820, 1002, 1010 and 1040. Form 483 issued.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Officers

- Issuing Officer

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