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FDA Inspection
•Spineology, Inc.•June 30, 2010

Spineology, Inc. – FDA Inspection, Jun 30, 2010

Record Details

This FDA Inspection record concerns Spineology, Inc., with an inspection on June 30, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Spineology, Inc.
Inspection Date
June 30, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e0d713e6-be32-467b-8ffe-590ff602aa59

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
667027
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of Spineology, Inc.

7
DateClassificationOfficeProject area
June 17, 2025NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 17, 2025NAIMinneapolis District OfficePostmarket Assurance: Medical Devices
February 15, 2022NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 12, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
March 31, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 7 other inspections on the company page
Other documents for Spineology, Inc.
  • FDA Inspection 1275322 - 2025-06-17
  • FDA Inspection 1267116 - 2025-04-17
  • FDA Inspection 1162392 - 2022-02-15
  • FDA Inspection 1071565 - 2018-10-12
  • FDA Inspection 1012390 - 2017-03-31

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