# 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/27c8f0ad-3694-413d-84fd-93574bca1454
Source feed: FDA_Inspections

> FDA inspection 1259798 of Remel Cleveland, a Division of Remel Inc., February 03, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259798
- Company Name: Remel Cleveland, a Division of Remel Inc.
- Inspection Date: 2025-02-03
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Cincinnati District Office
- 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/cincinnati-district-office/b67a0c35-82e3-4176-9039-988378f65c22