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FDA Inspection
•Groman Inc.•March 7, 2023

Groman Inc. – FDA Inspection, Mar 7, 2023

Record Details

This FDA Inspection record concerns Groman Inc., with an inspection on March 7, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Groman Inc.
Inspection Date
March 7, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Dianiris C. Ayala
View Company Profile

ID · f70689dd-24db-4901-b864-a88d4b9b73c0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1206335
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Groman Inc.

4
DateClassificationOfficeProject area
March 17, 2026NAICenter for Devices and Radiological HealthCompliance: Devices
March 5, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 10, 2015VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 3, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Groman Inc.
  • FDA Inspection 1308980 - 2026-03-17
  • FDA Inspection 1043954 - 2018-03-05
  • FDA Inspection 933478 - 2015-07-10
  • FDA Inspection 700357 - 2010-12-03

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