# Newman Medical – FDA Inspection, May 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/newman-medical/6fec244f-83f3-47a8-8a86-708ced54c59a
Source feed: FDA_Inspections

> FDA inspection 1091306 of Newman Medical, May 31, 2019. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091306
- Company Name: Newman Medical
- Inspection Date: 2019-05-31
- 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: 5

## Related Documents

- [FDA Inspection 1250110 - 2024-09-25](https://www.keypedia.com/records/fda_inspections/newman-medical/e9295a54-6dcb-47cd-b520-86eafc2531ac)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/vicky-l-cruz/282da571-56be-48f4-96c6-d590829b12c2)

Company: https://www.keypedia.com/companies/newman-medical/9ccbc85f-9be9-443e-850f-c5d99d5eefa6

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