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FDA Inspection
•Helena Laboratories, Inc•July 14, 2017

Helena Laboratories, Inc – FDA Inspection, Jul 14, 2017

Record Details

This FDA Inspection record concerns Helena Laboratories, Inc, with an inspection on July 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Helena Laboratories, Inc
Inspection Date
July 14, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Ellen J. Tave (Issuing Officer)
View Company Profile

ID · a34123e3-12c8-49d5-af1c-14993ba858c7

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1029048
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Helena Laboratories, Inc

2
DateClassificationOfficeProject area
March 1, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
October 28, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Helena Laboratories, Inc
  • FDA Inspection 820619 - 2013-03-01
  • FDA Inspection 695366 - 2010-10-28

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