# FDA Inspection 970679 - Sharp U.K. Manufacturing (SUKM) - May 03, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/sharp-uk-manufacturing-sukm/02a42c78-515f-4a8c-9a84-4844e32a9e4d
Source feed: FDA_Inspections

> FDA Inspection 970679 for Sharp U.K. Manufacturing (SUKM) on May 03, 2016. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 970679
- Company Name: Sharp U.K. Manufacturing (SUKM)
- Inspection Date: 2016-05-03
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1050399 - 2018-04-23](https://www.globalkeysolutions.net/records/fda_inspections/sharp-uk-manufacturing-sukm/f48a759b-563c-44e8-80b1-4f073238a18c)

Company: https://www.globalkeysolutions.net/companies/sharp-uk-manufacturing-sukm/2b48be2b-4595-41c2-b616-2af5bee1256a

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