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FDA Inspection
•Hinson and Hale Medical Technologies, Inc.•July 26, 2018

Hinson and Hale Medical Technologies, Inc. – FDA Inspection, Jul 26, 2018

Record Details

This FDA Inspection record concerns Hinson and Hale Medical Technologies, Inc., with an inspection on July 26, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Hinson and Hale Medical Technologies, Inc.
Inspection Date
July 26, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Gamal A. Norton (Issuing Officer)
View Company Profile

ID · ffd423d1-bcc4-448b-abab-580cf89fb172

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1060374
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.184Lack of or inadequate DHR procedures
  2. 21 CFR 820.30(b)Design plans - Lack of or inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Hinson and Hale Medical Technologies, Inc.

1
DateClassificationOfficeProject area
April 30, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Hinson and Hale Medical Technologies, Inc.
  • FDA Inspection 1087993 - 2019-04-30

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