# FDA Inspection 1013990 - Cefimeca - April 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/cefimeca/932a2d50-1a82-428a-b845-70daca9f791f
Source feed: FDA_Inspections

> FDA Inspection 1013990 for Cefimeca on April 26, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1013990
- Company Name: Cefimeca
- Inspection Date: 2017-04-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1270555 - 2025-05-23](https://www.keypedia.com/records/fda_inspections/cefimeca/45173f54-ca3b-4eab-834c-456fc364065c)
- [FDA Inspection 1270555 - 2025-05-23](https://www.keypedia.com/records/fda_inspections/cefimeca/7b3a80b8-8f1f-43fe-90e7-efbfa9128310)

Company: https://www.keypedia.com/companies/cefimeca/7a8a6dc3-ec9d-496e-a871-5340bafdb4a2

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