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FDA Inspection
•Haemonetics Corporation•August 31, 2017

Haemonetics Corporation – FDA Inspection, Aug 31, 2017

Record Details

This FDA Inspection record concerns Haemonetics Corporation, with an inspection on August 31, 2017, issued by the New England District Office, covering medical devices & rad health.

Company
Haemonetics Corporation
Inspection Date
August 31, 2017
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · a4465834-afc3-4936-9e23-e443c07c1964

Inspection Facts

Inspection number
1045923
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Haemonetics Corporation

3
DateClassificationOfficeProject area
December 20, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
February 7, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
September 19, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Haemonetics Corporation
  • FDA Inspection 1078708 - 2018-12-20
  • FDA Inspection 866083 - 2014-02-07
  • FDA Inspection 745197 - 2011-09-19

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