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FDA Inspection
•Gregory Manufacturing, Inc.•April 2, 2026

Gregory Manufacturing, Inc. – FDA Inspection, Apr 2, 2026

Record Details

This FDA Inspection record concerns Gregory Manufacturing, Inc., with an inspection on April 2, 2026, issued by the Center for Devices and Radiological Health, covering devices.

Company
Gregory Manufacturing, Inc.
Inspection Date
April 2, 2026
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Eric C. Schmitt (Issuing Officer)
View Company Profile

ID · e37027a3-7122-406e-b7ac-79166c3818a9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1311716
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. ISO 13485:2016 Clause 8.5.2Corrective action not taken

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Gregory Manufacturing, Inc.

3
DateClassificationOfficeProject area
November 21, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
September 12, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
September 21, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Gregory Manufacturing, Inc.
  • FDA Inspection 1075004 - 2018-11-21
  • FDA Inspection 896691 - 2014-09-12
  • FDA Inspection 747165 - 2011-09-21

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