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FDA establishment 3034656245, Prosper, Texas, United States. Part of Neurocareai (dba Savelife.ai)'s FDA records. Every inspection FDA has posted for the site, with its outcome and cited regulations.
Inspections: 1
Official action indicated: 0
Last inspection ended: Dec 12, 2025
Warning letters: 0
Inspections by Fiscal Year
FY2018 to FY2027 to date; 0 classified OAI
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
21 CFR 820.170(a). Lack of or inadequate instructions Installation instructions, inspection instructions and test procedures have not been adequately established.
21 CFR 820.22. Quality Audit/Reaudit - conducted Quality audits and reaudits have not been performed.
21 CFR 801.50(a). Labeling requirements for stand-alone software The stand-alone software that is regulated as a medical device did not provide its unique device identifier through either an easily readable plain-text statement displayed whenever the software is started or an easily readable plain-text statement displayed through a menu command.
21 CFR 820.50(a). Evaluation of suppliers, contractors, etc., requirements Requirements that must be met by suppliers, contractors and consultants have not been adequately established.
An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm.FDA Data Dashboard and warning letters
Prosper, Texas, United States. Part of