FDA Inspection
Remel Cleveland, a Division of Remel Inc.FDA Inspection 1009751 - Remel Cleveland, a Division of Remel Inc. - April 12, 2017
Record Details
This FDA Inspection record concerns Remel Cleveland, a Division of Remel Inc., with an inspection on April 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- April 12, 2017
- Product Type
- Devices
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ID · 70a45c1a-41ce-4634-8596-ea93edf4461b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1009751
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: 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 |
| March 16, 2010 | VAI | Center for Devices and Radiological Health | Compliance: 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 652081 - 2010-03-16
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