# FDA Inspection 1209531 - Trident SRL - June 08, 2023

Source: https://www.keypedia.com/records/fda_inspections/trident-srl/4f493777-974b-4ef5-9f83-660d53354cba
Source feed: FDA_Inspections

> FDA Inspection 1209531 for Trident SRL on June 08, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1209531
- Company Name: Trident SRL
- Inspection Date: 2023-06-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1209531 - 2023-06-08](https://www.keypedia.com/records/fda_inspections/trident-srl/83a9b4e8-504c-4109-a34a-895fcad4e739)

Company: https://www.keypedia.com/companies/trident-srl/ea09e324-3b1a-469b-9550-e96906d1f5e8

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