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FDA Inspection
•Greatbatch Medical•February 27, 2009

Greatbatch Medical – FDA Inspection, Feb 27, 2009

Record Details

This FDA Inspection record concerns Greatbatch Medical, with an inspection on February 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Greatbatch Medical
Inspection Date
February 27, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e751261b-db99-45aa-9f94-688f5d3ebd1d

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
572370
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of Greatbatch Medical

7
DateClassificationOfficeProject area
June 7, 2024Not classifiedMinneapolis District Office
May 23, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
May 25, 2016NAICenter for Devices and Radiological HealthBioresearch Monitoring
May 6, 2015NAICenter for Devices and Radiological HealthBioresearch Monitoring
March 18, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
View all 7 other inspections on the company page
Other documents for Greatbatch Medical
  • FDA Inspection 1236555 - 2024-06-07
  • FDA Inspection 1054275 - 2018-05-23
  • FDA Inspection 974240 - 2016-05-25
  • FDA Inspection 926242 - 2015-05-06
  • FDA Inspection 870467 - 2014-03-18

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