# Rubin & Poor, Inc. – FDA Inspection, Aug 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/rubin-poor-inc/7ea3296e-ff0e-496a-a18b-a9fcee3409f8
Source feed: FDA_Inspections

> FDA inspection 1021831 of Rubin & Poor, Inc., August 02, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021831
- Company Name: Rubin & Poor, Inc.
- Inspection Date: 2017-08-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1231261 - 2024-02-27](https://www.keypedia.com/records/fda_inspections/rubin-poor-inc/59159b76-24e6-40fe-9bfe-0b541cc76d38)
- FDA Inspection 727088 - 2011-05-26

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-h-smith/a78c3b20-1fb4-438f-904b-a6ab51a81945)

Company: https://www.keypedia.com/companies/rubin-poor-inc/b0b21989-ee0b-4479-ab4f-3dd2985c7333

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7