# FDA Inspection 1015943 - Ge Healthcare (Tianjin) Company - May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/ge-healthcare-tianjin-company/9e7339e2-a0ed-40a9-90ca-ae225fd8dd1d
Source feed: FDA_Inspections

> FDA Inspection 1015943 for Ge Healthcare (Tianjin) Company on May 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015943
- Company Name: Ge Healthcare (Tianjin) Company
- Inspection Date: 2017-05-25
- 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 1015943 - 2017-05-25](https://www.keypedia.com/records/fda_inspections/ge-healthcare-tianjin-company/88ee4545-1190-42e8-b271-f682a2e88a54)

Company: https://www.keypedia.com/companies/ge-healthcare-tianjin-company/3ccef64b-7bcc-4e26-80dc-41f1468c8771

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