# FDA Inspection 1025149 - Ethicon, Inc. - September 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/ethicon-inc/196d5a1d-e8d7-4de3-b893-33f427bcad2f
Source feed: FDA_Inspections

> FDA Inspection 1025149 for Ethicon, Inc. on September 14, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025149
- Company Name: Ethicon, Inc.
- Inspection Date: 2017-09-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 924375 - 2015-04-24](https://www.keypedia.com/records/fda_inspections/ethicon-inc/f0cd1ba7-a01b-406b-818f-6806032386f9)
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- [FDA Inspection 770318 - 2012-02-27](https://www.keypedia.com/records/fda_inspections/ethicon-inc/69a1d2ec-56f7-4fdf-b9d6-97689fdc0c5d)
- [FDA Inspection 770318 - 2012-02-27](https://www.keypedia.com/records/fda_inspections/ethicon-inc/323f941a-c314-4173-8967-fde554fd7236)

Company: https://www.keypedia.com/companies/ethicon-inc/ebaffaf1-02bb-4c94-a875-d3b954fcc2a7

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