# Pluromed, Inc. – FDA Inspection, Oct 9, 2012

Source: https://www.keypedia.com/records/fda_inspections/pluromed-inc/c33d6c6f-7220-438a-a101-d0eae1a8d165
Source feed: FDA_Inspections

> FDA inspection 810585 of Pluromed, Inc., October 09, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 810585
- Company Name: Pluromed, Inc.
- Inspection Date: 2012-10-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 730018 - 2011-05-24](https://www.keypedia.com/records/fda_inspections/pluromed-inc/e0ec7252-be9e-4a3e-9179-a28006f7b731)
- [FDA Inspection 715012 - 2011-03-11](https://www.keypedia.com/records/fda_inspections/pluromed-inc/ae583233-b078-4b0c-81d6-6988395d8835)

Company: https://www.keypedia.com/companies/pluromed-inc/a0da02d6-7cd8-432a-b342-4ddaae117d94

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