# Jensen Industries, Inc. – FDA Inspection, Mar 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/jensen-industries-inc/28194eb6-b8fb-44be-840b-db0cc5b86fe7
Source feed: FDA_Inspections

> FDA inspection 1006004 of Jensen Industries, Inc., March 21, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006004
- Company Name: Jensen Industries, Inc.
- Inspection Date: 2017-03-21
- 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 831783 - 2013-05-09
- FDA Inspection 611027 - 2009-09-03

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/eric-c-schmitt/f2716c8c-f06e-4519-a1e7-63a3ef6e07fb)

Company: https://www.keypedia.com/companies/jensen-industries-inc/56c79a00-106d-4ca5-8feb-feebaf8cad0d

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