# Creganna Medical – FDA Inspection, Nov 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/creganna-medical/e9a1525d-ecb8-4c51-84b6-4ed8ac903aa5
Source feed: FDA_Inspections

> FDA inspection 992606 of Creganna Medical, November 18, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 992606
- Company Name: Creganna Medical
- Inspection Date: 2016-11-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 870227 - 2014-02-20](https://www.keypedia.com/records/fda_inspections/creganna-medical/894c89d4-3fe5-4591-ac4d-141fcfacc980)

## Related Officers

- [Sargum C. Morgan](https://www.keypedia.com/people/sargum-c-morgan/a769e36a-3382-414a-b9b1-1ebc755c8392)

Company: https://www.keypedia.com/companies/creganna-medical/6f962936-7392-45a6-99ba-b00889f1e0bf

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