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Spinalight, Inc., Saint Petersburg, FL – FDA Inspections

Inspection records and compliance data for Spinalight, Inc. in Saint Petersburg, Florida. 4 FDA inspections on record (2 OAI), last inspected January 31, 2024.

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Company Profile

This profile covers Spinalight, Inc. based in Saint Petersburg, Florida, United States.

FDA Inspection History

FDA inspections
4
OAI
2
VAI
2
NAI
0
Form 483s
0
Warning letters
0

First inspected August 18, 2011. Last inspected January 31, 2024.

Most cited issue areas

  • Purchasing controls, Lack of or inadequate procedures3 inspections
  • Design control - no procedures2 inspections
  • DMR - not or inadequately maintained2 inspections

FDA inspections (4)

DateResultFDA center(s)Insp. #
January 31, 2024VAIMedical Devices & Rad Health · Compliance: Devices1228191
March 19, 2015VAIMedical Devices & Rad Health · Compliance: Devices919385
July 19, 2012OAIMedical Devices & Rad Health · Postmarket Assurance: Devices792598
August 18, 2011OAIMedical Devices & Rad Health · Postmarket Assurance: Devices740084
FDA documents

No Form 483s, Warning Letters or EIRs on record.

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Florida Probe Corporation
Company Information

Name

Spinalight, Inc.

FEI Number

3006315109

Address

2201 62nd Ave N, Saint Petersburg, Florida 33702, United States

Country

United States

ID: a41339f9-3026-4de3-822f-20d0e6a4fba2

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