Spinalight, Inc.

Form 483

Saint Petersburg, Florida, United StatesFEI 3006315109Issued July 19, 2012

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3006315109.

Observations7

Issue DateJuly 19, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Spinalight, Inc.
Location: Saint Petersburg, Florida, United States
FEI Number: 3006315109
Product Type: Devices
Issue Date: July 19, 2012
Country: United States

Inspection History, 2011 to 2024

VAI2

OAI2

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Spinalight, Inc. FDA Form 483, Saint Petersburg, Florida, July 19, 2012