# FDA Inspection 626466 - DePuy Mitek, Inc., a Johnson & Johnson Co. - October 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/depuy-mitek-inc-a-johnson-johnson-co/9279b830-0627-46c4-8aed-d437ba3f89dd
Source feed: FDA_Inspections

> FDA Inspection 626466 for DePuy Mitek, Inc., a Johnson & Johnson Co. on October 22, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 626466
- Company Name: DePuy Mitek, Inc., a Johnson & Johnson Co.
- Inspection Date: 2009-10-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 821194 - 2013-03-06](https://www.keypedia.com/records/fda_inspections/depuy-mitek-inc-a-johnson-johnson-co/e14d3373-ab1b-4489-8051-682e3fd650d4)
- [FDA Inspection 626466 - 2009-10-22](https://www.keypedia.com/records/fda_inspections/depuy-mitek-inc-a-johnson-johnson-co/cf504493-ea96-4b31-a41b-a63848041cd8)

Company: https://www.keypedia.com/companies/depuy-mitek-inc-a-johnson-johnson-co/a7e18af9-1345-4258-ad39-43a79c1959f4

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