# FDA Inspection 1061483 - Celfa s.c. - July 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/celfa-sc/a69cda2f-19e2-4a12-ba4f-c2ceb250936d
Source feed: FDA_Inspections

> FDA Inspection 1061483 for Celfa s.c. on July 20, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061483
- Company Name: Celfa 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 1061483 - 2018-07-20](https://www.globalkeysolutions.net/records/fda_inspections/celfa-sc/d14d6808-de9d-4a37-af89-f32667b3cbe1)

Company: https://www.globalkeysolutions.net/companies/celfa-sc/22da8ec0-ed7f-46f0-b149-cc6e7b11ebc8

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