# FDA Inspection 1021889 - NuPak Medical, Ltd - April 27, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/nupak-medical-ltd/2a32bb9c-a01c-43c8-89c0-15d8a32ec12d
Source feed: FDA_Inspections

> FDA Inspection 1021889 for NuPak Medical, Ltd on April 27, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021889
- Company Name: NuPak Medical, Ltd
- Inspection Date: 2017-04-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1021889 - 2017-04-27](https://www.globalkeysolutions.net/records/fda_inspections/nupak-medical-ltd/fa986fe6-75f2-42f6-8a63-cfe0a513113f)

Company: https://www.globalkeysolutions.net/companies/nupak-medical-ltd/5f4aca0d-a662-411e-bfd1-3797d63c1115

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