# Fricke Dental MFG, Co – FDA Inspection, Jun 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/fricke-dental-mfg-co/693f10db-59a6-4d49-b66d-db233a1a8dfb
Source feed: FDA_Inspections

> FDA inspection 977019 of Fricke Dental MFG, Co, June 16, 2016. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977019
- Company Name: Fricke Dental MFG, Co
- Inspection Date: 2016-06-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1073322 - 2018-11-14
- [FDA Inspection 836178 - 2013-06-18](https://www.keypedia.com/records/fda_inspections/fricke-dental-mfg-co/96f093c0-5440-4b1d-9659-c30110238171)
- [FDA Inspection 714151 - 2011-03-09](https://www.keypedia.com/records/fda_inspections/fricke-dental-mfg-co/a3b6b770-305c-4573-92e8-10b16fffc989)
- FDA Inspection 596469 - 2009-05-19

Company: https://www.keypedia.com/companies/fricke-dental-mfg-co/a09ae47b-1bc9-4b04-985c-a34111ea85c1

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