# FDA Inspection 1030320 - GNJ Ent Inc - October 27, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/gnj-ent-inc/17260f0b-3a61-4e1a-9e77-edec4295f79e
Source feed: FDA_Inspections

> FDA Inspection 1030320 for GNJ Ent Inc on October 27, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030320
- Company Name: GNJ Ent Inc
- Inspection Date: 2017-10-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 927940 - 2015-06-10](https://www.globalkeysolutions.net/records/fda_inspections/gnj-ent-inc/efdbfc86-6792-45e4-a3b6-901484b8b879)
- [FDA Inspection 927940 - 2015-06-10](https://www.globalkeysolutions.net/records/fda_inspections/gnj-ent-inc/20581037-3efb-4753-9256-63f6d12ae72a)
- [FDA Inspection 737984 - 2011-07-22](https://www.globalkeysolutions.net/records/fda_inspections/gnj-ent-inc/9a4c4233-2e8f-415b-aea7-61f78657db46)

Company: https://www.globalkeysolutions.net/companies/gnj-ent-inc/dc51af3e-42a6-4411-966e-ba4dba2d148e

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