# FDA Inspection 1235538 - Efer Endoscopy - April 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/efer-endoscopy/3647e9ab-b9b9-46dd-a561-55f1aed7917f
Source feed: FDA_Inspections

> FDA Inspection 1235538 for Efer Endoscopy on April 05, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1235538
- Company Name: Efer Endoscopy
- Inspection Date: 2024-04-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1235538 - 2024-04-05](https://www.keypedia.com/records/fda_inspections/efer-endoscopy/55dd1b13-919c-4106-860d-be459966d8f8)

Company: https://www.keypedia.com/companies/efer-endoscopy/b5adc865-d262-4234-ba3b-2373543dfc66

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