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FDA Inspection
•Canyon Rush, LLC•May 15, 2026

Canyon Rush, LLC – FDA Inspection, May 15, 2026

Record Details

This FDA Inspection record concerns Canyon Rush, LLC, with an inspection on May 15, 2026, issued by the New York District Office, covering human drugs.

Company
Canyon Rush, LLC
Inspection Date
May 15, 2026
Product Type
Human Drugs
Office
New York District Office
Person
  • Lauren H. Augustyniak (Issuing Officer)
View Company Profile

ID · d7e58e17-bcb0-48b8-8a19-4a5c93fe3938

Inspection Facts

Inspection number
1317524
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.160(a)Following/documenting laboratory controls
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.194(a)Complete test data included in records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Canyon Rush, LLC

7
DateClassificationOfficeProject area
August 23, 2024Not classifiedNew York District Office
April 15, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 27, 2021NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
May 4, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
October 9, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Canyon Rush, LLC
  • FDA Inspection 1247920 - 2024-08-23
  • FDA Inspection 1167126 - 2022-04-15
  • FDA Inspection 1142658 - 2021-05-27
  • FDA Inspection 969391 - 2016-05-04
  • FDA Inspection 900822 - 2014-10-09

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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