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FDA Inspection
•Tarry Medical Products, Inc.•October 9, 2025

Tarry Medical Products, Inc. – FDA Inspection, Oct 9, 2025

Record Details

This FDA Inspection record concerns Tarry Medical Products, Inc., with an inspection on October 9, 2025, issued by the New England District Office, covering human drugs.

Company
Tarry Medical Products, Inc.
Inspection Date
October 9, 2025
Product Type
Human Drugs
Office
New England District Office
People
  • Josh Renzo N. Ramilo (Issuing Officer)
  • Martin M. Kimani (Investigator)
View Company Profile

ID · 29ae1459-fb2f-4ae1-b8f4-de28ce1ad594

Inspection Facts

Inspection number
1279115
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

3
  1. 21 CFR 211.166(a)Results not used for expiration dates, storage cond.
  2. 21 CFR 211.192Investigations of discrepancies, failures
  3. 21 CFR 211.22(a)Approve or reject components, products

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Tarry Medical Products, Inc.

4
DateClassificationOfficeProject area
March 3, 2026NAINew England District OfficePostmarket Assurance: Medical Devices
September 27, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
May 30, 2022NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
October 15, 2015VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Tarry Medical Products, Inc.
  • FDA Inspection 1282936 - 2026-03-03
  • FDA Inspection 1219494 - 2023-09-27
  • FDA Inspection 1171323 - 2022-05-30
  • FDA Inspection 947601 - 2015-10-15

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