# FDA Inspection 1110500 - Remel Cleveland, a Division of Remel Inc. - November 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/remel-cleveland-a-division-of-remel-inc/996fae76-fbab-4d1e-b6e1-72a9df3e3f8c
Source feed: FDA_Inspections

> FDA inspection 1110500 of Remel Cleveland, a Division of Remel Inc., November 20, 2019. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1110500
- Company Name: Remel Cleveland, a Division of Remel Inc.
- Inspection Date: 2019-11-20
- 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: 0

## Related Documents

- [FDA Inspection 1259798 - 2025-02-03](https://www.keypedia.com/records/fda_inspections/remel-cleveland-a-division-of-remel-inc/27c8f0ad-3694-413d-84fd-93574bca1454)
- [FDA Inspection 1009751 - 2017-04-12](https://www.keypedia.com/records/fda_inspections/remel-cleveland-a-division-of-remel-inc/eb57aaa3-e57d-48d8-a506-cfdcaab817f1)
- FDA Inspection 652081 - 2010-03-16

Company: https://www.keypedia.com/companies/remel-cleveland-a-division-of-remel-inc/021debca-74ec-4d32-b2e1-1766d4b852d2

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