Gorilla Mind LLC

FDA Regulatory Profile

Gorilla Mind LLC appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (F-0053-2025, Class I) was initiated on Sep 6, 2024. Its most recent FDA inspection ended on May 5, 2026 (No Action Indicated (NAI)).

Reviewing Gorilla Mind LLC as a supplier? Get its full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
F-0053-2025Class IGorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased EnergySep 6, 2024

Recent FDA Inspections

DateSiteProductClassificationFEI
May 5, 2026Meridian, IDFood/CosmeticsNo Action Indicated (NAI)3014084547

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).