# FDA Inspection 992922 - Hi-Dow International Inc - November 28, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/hi-dow-international-inc/25c50037-9a39-4f97-af3f-046ce91507ca
Source feed: FDA_Inspections

> FDA Inspection 992922 for Hi-Dow International Inc on November 28, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992922
- Company Name: Hi-Dow International Inc
- Inspection Date: 2016-11-28
- Classification: Voluntary Action Indicated (VAI)
- 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/hi-dow-international-inc/7aaaa08a-dcd7-4643-9578-cf2f0ff6195c

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