# DePuy Bridgewater – FDA Inspection, Oct 2, 2012

Source: https://www.keypedia.com/records/fda_inspections/depuy-bridgewater/bed28730-bf4a-4fcf-9ebf-702f26060ca2
Source feed: FDA_Inspections

> FDA inspection 801053 of DePuy Bridgewater, October 02, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 801053
- Company Name: DePuy Bridgewater
- Inspection Date: 2012-10-02
- 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: 1

## Related Documents

- FDA Inspection 729349 - 2011-06-13
- FDA Inspection 713061 - 2011-03-08
- FDA Inspection 629365 - 2009-11-19
- FDA Inspection 582091 - 2009-05-08
- FDA Inspection 582090 - 2009-05-08

Company: https://www.keypedia.com/companies/depuy-bridgewater/60a1f72e-a6b4-4119-bcfe-bf5d4aebb162

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