# FDA Inspection 1069270 - Makeblock Co. Ltd. - December 07, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/makeblock-co-ltd/d76a9265-f8a7-4d76-9c78-2a9a4c6e7685
Source feed: FDA_Inspections

> FDA Inspection 1069270 for Makeblock Co. Ltd. on December 07, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069270
- Company Name: Makeblock Co. Ltd.
- Inspection Date: 2017-12-07
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/makeblock-co-ltd/7192057c-af05-42df-8ac7-91eb3d90d2a9

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