# FDA Inspection 920341 - Sunwell Biotech Co Ltd - March 05, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/sunwell-biotech-co-ltd/dcb3f35b-5551-41d2-b45b-64d6d33579f0
Source feed: FDA_Inspections

> FDA Inspection 920341 for Sunwell Biotech Co Ltd on March 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920341
- Company Name: Sunwell Biotech Co Ltd
- Inspection Date: 2015-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 920341 - 2015-03-05](https://www.globalkeysolutions.net/records/fda_inspections/sunwell-biotech-co-ltd/bdf07318-de34-4078-a6bb-a03ffcd75563)

Company: https://www.globalkeysolutions.net/companies/sunwell-biotech-co-ltd/dbbea9b7-9f4b-4f69-99c7-cdcef681a36a

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