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Scilex Pharmaceuticals Inc. Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed 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 this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3020017292.

Scilex Pharmaceuticals Inc.

Palo Alto, California, United States
Issue DateMay 20, 2026
FEI Number3020017292
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Scilex Pharmaceuticals Inc. FDA Form 483, Palo Alto, California, May 20, 2026