FDA Inspection
Haemonetics CorporationHaemonetics Corporation – FDA Inspection, May 3, 2013
Record Details
This FDA Inspection record concerns Haemonetics Corporation, with an inspection on May 3, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Haemonetics Corporation
- Inspection Date
- May 3, 2013
- Product Type
- Devices
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ID · fe17a70c-13c1-454d-b3c4-842242fcf3b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 830220
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
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Other FDA inspections of Haemonetics Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 18, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Haemonetics Corporation
- FDA Inspection 676450 - 2010-08-18
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