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FDA Inspection
•Intai Technology Corp. Implants Business Unit•September 11, 2025

Intai Technology Corp. Implants Business Unit – FDA Inspection, Sep 11, 2025

Record Details

This FDA Inspection record concerns Intai Technology Corp. Implants Business Unit, with an inspection on September 11, 2025, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Intai Technology Corp. Implants Business Unit
Inspection Date
September 11, 2025
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Christina D. Mello (Issuing Officer)
View Company Profile

ID · 27608a39-930e-4d42-9127-5e9f9d4e4b0e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1281748
FDA center
Medical Devices & Rad Health
Project area
Compliance: Medical Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.50(a)(2)Supplier oversight

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Intai Technology Corp. Implants Business Unit

1
DateClassificationOfficeProject area
March 16, 2017Not classifiedOffice of Inspections and InvestigationsCompliance: Devices
Other documents for Intai Technology Corp. Implants Business Unit
  • FDA Inspection 1008951 - 2017-03-16

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