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Agebox — FDA Facility Profile

FEI 3038759360

Agebox (FEI 3038759360) located in Wilmington, DE, United States has FDA compliance records.

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What FDA found at this site

Inspections on record
None in FDA's published inspection data
Warning letters
1 listed by FDA for this FEI, latest Dec 19, 2025
Recalls as the recalling firm
1, latest Oct 28, 2025

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Oct 28, 2025Not yet classifiedD-0344-2026Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively… and 1 more product
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Facility details

Location
Wilmington, DE (United States)

Compliance actions

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.