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FDA Inspection
•Tarry Medical Products, Inc.•October 15, 2015

Tarry Medical Products, Inc. – FDA Inspection, Oct 15, 2015

Record Details

This FDA Inspection record concerns Tarry Medical Products, Inc., with an inspection on October 15, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Tarry Medical Products, Inc.
Inspection Date
October 15, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e61b09f0-639c-4232-adb4-291cbb12b26a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
947601
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

5
  1. 21 CFR 820.181DMR - not or inadequately maintained
  2. 21 CFR 820.30(g)Design validation- Lack of or inadequate procedures
  3. 21 CFR 820.198(a)Lack of or inadequate complaint procedures
  4. 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
  5. 21 CFR 803.17(b)(1)Info evaluated to determine if event was reportable

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
October 9, 2025Not classifiedNew England District OfficeDrug Quality Assurance
September 27, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
May 30, 2022NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
Other documents for Tarry Medical Products, Inc.
  • FDA Inspection 1282936 - 2026-03-03
  • FDA Inspection 1279115 - 2025-10-09
  • FDA Inspection 1219494 - 2023-09-27
  • FDA Inspection 1171323 - 2022-05-30

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