Tyler R. Courtney

FDA investigator

Appears on 4 documents from 2019 to 2026, mostly at sites in Minnesota. Most often cites corrective and preventive action (21 CFR 820.100).

4
Documents on file
3.5
Observations per 483
2019
First seen
2026
Most recent

What they cite most

From 14 observations
  • 21 CFR 820.100
    Corrective and preventive action
    2
  • 21 CFR 820.25(b)
    Personnel
    2
  • ISO 13485:2016 Clause 7.1
    Scope
    1
  • ISO 13485:2016 Clause 7.3.9
    Definitions
    1
  • 21 CFR 801.40(a)
    Form of a unique device identifier
    1
  • 21 CFR 803.17
    What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
    1

Activity by year

2019: 1, 2022: 1, 2024: 1, 2026: 1

Where

Minnesota 3 · North Carolina 1

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Inspection history

4 documents, newest first
FirmOpen
483 Form 483 · FEI 3002619777Feb 9, 2026 · Eagan, Minnesota
483 AbleNetJul 8, 2024 · Roseville, Minnesota
483 Aurolife Pharma LLCAug 26, 2022 · Durham, North Carolina
483 Minnesota MedTec, Inc.Dec 11, 2019 · Maple Grove, Minnesota

About this profile

What does Tyler R. Courtney inspect?

Tyler R. Courtney appears on 4 documents on file covering 4 sites, mostly in Minnesota.

What do they cite most often?

21 CFR 820.100 (corrective and preventive action), followed by 21 CFR 820.25(b) and ISO 13485:2016 Clause 7.1.

Can I read the observations?

Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.

How current is this profile?

The most recent document on file for Tyler R. Courtney is dated Feb 9, 2026.