# FDA Inspection 830220 - Haemonetics Corporation - May 03, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/haemonetics-corporation/fe17a70c-13c1-454d-b3c4-842242fcf3b1/
Source feed: FDA_Inspections

> FDA Inspection 830220 for Haemonetics Corporation on May 03, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830220
- Company Name: Haemonetics Corporation
- Inspection Date: 2013-05-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 676450 - 2010-08-18](https://www.globalkeysolutions.net/api/records/fda_inspections/haemonetics-corporation/7530ebc8-2684-49d9-9cfc-f58ea40079bc/)

Company: https://www.globalkeysolutions.net/companies/haemonetics-corporation/c9d26970-837b-421a-bf7e-6479a7da57ad

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