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FDA Inspection
•Neurogan, Inc.•April 17, 2026

Neurogan, Inc. – FDA Inspection, Apr 17, 2026

Record Details

This FDA Inspection record concerns Neurogan, Inc., with an inspection on April 17, 2026, issued by the Los Angeles District Office, covering foods & cosmetics.

Company
Neurogan, Inc.
Inspection Date
April 17, 2026
Product Type
Foods & Cosmetics
Office
Los Angeles District Office
Person
  • Gerard D. Difiore (Issuing Officer)
View Company Profile

ID · 7076872c-2aa3-4280-bab7-13e782d70e68

Inspection Facts

Inspection number
1312864
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ
Outcome
Form 483 issued

FDA Citations

13
  1. 21 CFR 111.110Quality control - Laboratory control processes; production, process control
  2. 21 CFR 111.123(a)(8)Quality control - finished batch, distribution
  3. 21 CFR 111.210Master manufacturing record - record requirements
  4. 21 CFR 111.255(b)Batch record - complete
  5. 21 CFR 111.27(a)Equipment - design - appropriate and suitable
  6. 21 CFR 111.315(b)Sampling plans; establish, follow
  7. 21 CFR 111.403Written procedures - establish; packaging & labeling
  8. 21 CFR 111.410(b)Label, packaging - discrepancies
  9. 21 CFR 111.503Written procedures - establish; returned dietary supplements
  10. 21 CFR 111.560(a)Product complaint - qualified person review & investigate

Showing 10 of 13 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Neurogan, Inc.

1
DateClassificationOfficeProject area
June 5, 2019VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
Other documents for Neurogan, Inc.
  • FDA Inspection 1091956 - 2019-06-05

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