# FDA Inspection 971941 - A. R. Hinkel Company, Inc. dba R.A.Fischer - June 06, 2016

Source: https://www.keypedia.com/records/fda_inspections/a-r-hinkel-company-inc-dba-rafischer/f15c90a7-6f66-4f06-8cb6-caf0499cf59c
Source feed: FDA_Inspections

> FDA Inspection 971941 for A. R. Hinkel Company, Inc. dba R.A.Fischer on June 06, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971941
- Company Name: A. R. Hinkel Company, Inc. dba R.A.Fischer
- Inspection Date: 2016-06-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/a-r-hinkel-company-inc-dba-rafischer/3383d00c-e8b8-41a2-9866-414d47c338be

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