# FDA Inspection 972671 - George Tiemann & Co. - June 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/george-tiemann-co/15599f71-5b1a-4516-bf58-231a59de962b
Source feed: FDA_Inspections

> FDA Inspection 972671 for George Tiemann & Co. on June 01, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 972671
- Company Name: George Tiemann & Co.
- Inspection Date: 2016-06-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/george-tiemann-co/4a89b928-7792-4bc8-8dda-3fa1e0ac2608

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