# DPM USA Corp. – FDA Inspection, Dec 7, 2012

Source: https://www.keypedia.com/records/fda_inspections/dpm-usa-corp/c1f8934c-b9d1-456d-8e8b-1afc42492911
Source feed: FDA_Inspections

> FDA inspection 810097 of DPM USA Corp., December 07, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 810097
- Company Name: DPM USA Corp.
- Inspection Date: 2012-12-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1052326 - 2018-02-28
- [FDA Inspection 896209 - 2014-09-15](https://www.keypedia.com/records/fda_inspections/dpm-usa-corp/b49b2d94-4dcf-4a9b-b1fe-42cf8e1abca9)

Company: https://www.keypedia.com/companies/dpm-usa-corp/836cd82a-9cf8-4932-a05d-2c5d865d78cc

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