FDA Inspection
CLARITY DESIGN, INC.CLARITY DESIGN, INC. – FDA Inspection, Jul 10, 2024
Record Details
This FDA Inspection record concerns CLARITY DESIGN, INC., with an inspection on July 10, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 26c8b044-727b-4253-96c2-74128a9e6dae
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1243535
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.
- 21 CFR 820.70(g)(2)Periodic equipment inspection lack of or inadequate procedu
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of CLARITY DESIGN, INC.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 9, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for CLARITY DESIGN, INC.
- FDA Inspection 1038643 - 2018-01-09
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