# Helmer Inc. – FDA Inspection, Jul 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/helmer-inc/fb5b16f5-6199-4c5b-abe1-5666bd716d4a
Source feed: FDA_Inspections

> FDA inspection 1020923 of Helmer Inc., July 31, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020923
- Company Name: Helmer Inc.
- Inspection Date: 2017-07-31
- 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: 3

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- [FDA Inspection 735937 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/helmer-inc/eb08adf7-52a6-471e-a686-e32fbbb95b86)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/joseph-r-strelnik/1fb7d50e-abf2-45ef-85a8-71c61b33e42d)

Company: https://www.keypedia.com/companies/helmer-inc/7bd9fd06-55ce-4e4f-91d3-dff47dd789ec

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