FDA Inspection
Rubin & Poor, Inc.Rubin & Poor, Inc. – FDA Inspection, Feb 27, 2024
Record Details
This FDA Inspection record concerns Rubin & Poor, Inc., with an inspection on February 27, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 59159b76-24e6-40fe-9bfe-0b541cc76d38
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1231261
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
- 21 CFR 801.20(a)Label to bear a unique device identifier
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Other FDA inspections of Rubin & Poor, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 2, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 26, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Rubin & Poor, Inc.
- FDA Inspection 1021831 - 2017-08-02
- FDA Inspection 727088 - 2011-05-26
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