# FDA Inspection 1051637 - Regen Lab Sa - March 15, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/regen-lab-sa/558c1cbf-deaa-4296-a555-7b754a41ccb3
Source feed: FDA_Inspections

> FDA Inspection 1051637 for Regen Lab Sa on March 15, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1051637
- Company Name: Regen Lab Sa
- Inspection Date: 2018-03-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051637 - 2018-03-15](https://www.globalkeysolutions.net/records/fda_inspections/regen-lab-sa/5ce3f4f3-7a7f-44d6-af21-670d2e7ee7d8)
- [FDA Inspection 878719 - 2014-04-17](https://www.globalkeysolutions.net/records/fda_inspections/regen-lab-sa/2774c4d1-08c1-4452-8fa1-2c9b33667604)

Company: https://www.globalkeysolutions.net/companies/regen-lab-sa/6605b711-2d60-47c1-8586-b3cdcb1e4caf

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