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FDA Inspection 1262634 — Spryson America Inc.

Spryson America Inc. — FEI 2519945

The FDA completed an inspection of Spryson America Inc. on February 25, 2025 in Pittsburgh, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Pittsburgh, PA (United States)

Facility

Other inspections at this facility

  • 1181451 (VAI Thu Oct 13 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1095111 (NAI Tue Jul 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984418 (NAI Thu Apr 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 832575 (NAI Fri May 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 657532 (NAI Tue Apr 20 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources