# FDA Inspection 1246096 - Nightware - July 01, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/nightware/b064dc9d-23c7-45f8-9eb1-4a70fa804b13
Source feed: FDA_Inspections

> FDA Inspection 1246096 for Nightware on July 01, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1246096
- Company Name: Nightware
- Inspection Date: 2024-07-01
- 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 1246096 - 2024-07-01](https://www.globalkeysolutions.net/records/fda_inspections/nightware/e2a261ae-1067-46ce-89d4-7a8fb5d48f23)

Company: https://www.globalkeysolutions.net/companies/nightware/58a30aa4-a255-49a1-9c4d-b9379cc9512d

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