# GNJ Ent Inc – FDA Inspection, Oct 27, 2017

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

> FDA inspection 1030320 of GNJ Ent Inc, October 27, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 927940 - 2015-06-10](https://www.keypedia.com/records/fda_inspections/gnj-ent-inc/efdbfc86-6792-45e4-a3b6-901484b8b879)
- [FDA Inspection 737984 - 2011-07-22](https://www.keypedia.com/records/fda_inspections/gnj-ent-inc/9a4c4233-2e8f-415b-aea7-61f78657db46)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

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

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