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FDA Inspection
•Green Star Labs, Inc.•August 25, 2026

Green Star Labs, Inc. – FDA Inspection, Aug 25, 2026

Record Details

This FDA Inspection record concerns Green Star Labs, Inc., with an inspection on August 25, 2026, issued by the Los Angeles District Office, covering human drugs.

Company
Green Star Labs, Inc.
Inspection Date
August 25, 2026
Product Type
Human Drugs
Office
Los Angeles District Office
People
  • Alexandra A. Cole (Issuing Officer)
  • Journey V Cordero (Issuing Officer)
  • Michael Araneta (Company Rep)
View Company Profile

ID · 2e94a660-37b9-4594-8301-d5ab6fe72fe2

Inspection Facts

Inspection number
1332668
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

9
  1. 21 CFR 211.100(a)Absence of Written Procedures
  2. 21 CFR 211.130(e)Packaging line inspection before use
  3. 21 CFR 211.142Written warehousing procedures established/followed
  4. 21 CFR 211.165(a)Testing and release for distribution
  5. 21 CFR 211.166(a)Lack of written stability program
  6. 21 CFR 211.198(a)Complaint Handling Procedure
  7. 21 CFR 211.22(d)Procedures not in writing, fully followed
  8. 21 CFR 211.63Equipment Design, Size and Location
  9. 21 CFR 211.84(d)(1)Component identity verification

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Green Star Labs, Inc.

2
DateClassificationOfficeProject area
July 6, 2026NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
February 14, 2025VAILos Angeles District OfficeFood Composition, Standards, Labeling, and Economics
Other documents for Green Star Labs, Inc.
  • FDA Inspection 1325566 - 2026-07-06
  • FDA Inspection 1261599 - 2025-02-14

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