FDA Inspection
Remel Cleveland, a Division of Remel Inc.FDA Inspection 652081 - Remel Cleveland, a Division of Remel Inc. - March 16, 2010
Record Details
This FDA Inspection record concerns Remel Cleveland, a Division of Remel Inc., with an inspection on March 16, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 16, 2010
- Product Type
- Devices
View Company Profile
ID · 1fe82c37-0028-4509-a2e7-9e3d6145fbdc
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 652081
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Remel Cleveland, a Division of Remel Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2025 | NAI | Cincinnati District Office | Postmarket Assurance: Medical Devices |
| November 20, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 12, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Remel Cleveland, a Division of Remel Inc.
- FDA Inspection 1259798 - 2025-02-03
- FDA Inspection 1110500 - 2019-11-20
- FDA Inspection 1009751 - 2017-04-12
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