# FDA Inspection 1061484 - Cefla s.c. - July 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/cefla-sc/76898dd8-138c-4de2-9013-53df00f88fed
Source feed: FDA_Inspections

> FDA Inspection 1061484 for Cefla s.c. on July 20, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1061484
- Company Name: Cefla s.c.
- Inspection Date: 2018-07-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1061484 - 2018-07-20](https://www.globalkeysolutions.net/records/fda_inspections/cefla-sc/e936978a-9c3f-4ae3-94d7-fc85fb192b72)
- [FDA Inspection 1061484 - 2018-07-20](https://www.globalkeysolutions.net/records/fda_inspections/cefla-sc/4d28c8a9-1f5a-4079-959a-b74950bf23e1)

Company: https://www.globalkeysolutions.net/companies/cefla-sc/ebcabe5c-f897-4c1b-b4f8-7a289bcc1987

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