# FDA Inspection 1020923 - Helmer Inc. - July 31, 2017

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

> FDA Inspection 1020923 for Helmer Inc. on July 31, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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