# FDA Inspection 1054421 - Rijuven Corporation - March 28, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/rijuven-corporation/c10228c4-1ce1-4953-a2e3-f1d80ac9b7cf
Source feed: FDA_Inspections

> FDA Inspection 1054421 for Rijuven Corporation on March 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054421
- Company Name: Rijuven Corporation
- Inspection Date: 2018-03-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1054421 - 2018-03-28](https://www.globalkeysolutions.net/records/fda_inspections/rijuven-corporation/23f55d93-1223-4342-9072-05d27f2fb0c4)

Company: https://www.globalkeysolutions.net/companies/rijuven-corporation/43d45c2f-a9ee-4be2-abc2-6b01ecbf0225

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