# Medela Inc – FDA Inspection, Jan 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/medela-inc/24aabd2f-d3a0-4cee-a0fe-9dca9539051b
Source feed: FDA_Inspections

> FDA inspection 648376 of Medela Inc, January 21, 2010. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 648376
- Company Name: Medela Inc
- Inspection Date: 2010-01-21
- 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: 7

## Related Documents

- FDA Inspection 893426 - 2014-08-27
- FDA Inspection 869654 - 2014-02-26
- [FDA Inspection 779907 - 2012-05-25](https://www.keypedia.com/records/fda_inspections/medela-inc/8a16c277-9263-41cb-b9ed-86b653a8c391)
- FDA Inspection 755250 - 2011-11-21
- FDA Inspection 747437 - 2011-08-09

Company: https://www.keypedia.com/companies/medela-inc/c3a05e54-356f-4189-94af-b0e6246c6dbd

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