# FDA Inspection 1276873 - Gener8 - July 29, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/gener8/082a41c7-5931-48bb-ad01-348b3cfee0b8
Source feed: FDA_Inspections

> FDA Inspection 1276873 for Gener8 on July 29, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276873
- Company Name: Gener8
- Inspection Date: 2025-07-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276873 - 2025-07-29](https://www.globalkeysolutions.net/records/fda_inspections/gener8/2b9fb9b5-494f-4ba6-be42-268a7969a0ac)
- [FDA Inspection 1276873 - 2025-07-29](https://www.globalkeysolutions.net/records/fda_inspections/gener8/59f78da0-e910-4199-943b-8e4cc75d6499)

Company: https://www.globalkeysolutions.net/companies/gener8/bc8384a9-3f8f-44f1-9960-40f550abbb96

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