# G21 Srl – FDA Inspection, May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/g21-srl/d37cb158-0327-4fc9-80fb-a914889dc1b2
Source feed: FDA_Inspections

> FDA inspection 1012795 of G21 Srl, May 25, 2017. Classification: No Action Indicated (NAI). 4 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: 1012795
- Company Name: G21 Srl
- Inspection Date: 2017-05-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1273678 - 2025-05-21
- FDA Inspection 1194285 - 2022-12-01

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)

Company: https://www.keypedia.com/companies/g21-srl/58712362-8a0f-4f58-abcd-0b45fa44b977

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