# FDA Inspection 1259798 - Remel Cleveland, a Division of Remel Inc. - February 03, 2025

Source: https://www.keypedia.com/records/fda_inspections/remel-cleveland-a-division-of-remel-inc/93e3bd94-67bd-4360-bb99-43d8370922ba
Source feed: FDA_Inspections

> FDA inspection 1259798 of Remel Cleveland, a Division of Remel Inc., February 03, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1259798
- Company Name: Remel Cleveland, a Division of Remel Inc.
- Inspection Date: 2025-02-03
- 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: 2

## Related Documents

- FDA Inspection 1110500 - 2019-11-20
- [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

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

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