# FDA Inspection 1089433 - RST-Sanexas - April 02, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/rst-sanexas/808fe045-474f-435e-a8e0-05a34466a020
Source feed: FDA_Inspections

> FDA Inspection 1089433 for RST-Sanexas on April 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089433
- Company Name: RST-Sanexas
- Inspection Date: 2019-04-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1089433 - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/rst-sanexas/08891990-b432-4a21-a4f9-72156566d426)

Company: https://www.globalkeysolutions.net/companies/rst-sanexas/63f5ef87-3b1a-4229-8445-8fd7cc1617ac

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