Alicia U. Jacobo

FDA investigator

Appears on 4 documents from 2024 to 2026, mostly at sites in Minnesota. Most often cites what are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me? (21 CFR 803.17).

4
Documents on file
3.0
Observations per 483
2024
First seen
2026
Most recent

What they cite most

From 12 observations
  • 21 CFR 803.17
    What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
    2
  • 21 CFR 820.198
    Complaint files
    2
  • ISO 13485:2016 Clause 4.1.1
    What is the scope of this subpart?
    1
  • ISO 13485:2016 Clause 7.1
    Scope
    1
  • ISO 13485:2016 Clause 7.5.6
    1
  • 21 CFR 820.100(a)
    Corrective and preventive action
    1

Activity by year

2024: 1, 2025: 1, 2026: 2

Where

Minnesota 3

Often inspects with

Tyler R. Courtney

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Inspection history

4 documents, newest first
FirmOpen
483 Production Systems, IncMar 12, 2026 · Shoreview, Minnesota
483 Seacole-CRC, LLCFeb 13, 2026 · Plymouth, Minnesota
483 INSPIRE MEDICAL SYSTEMS INCDec 19, 2025
483 AbleNetJul 8, 2024 · Roseville, Minnesota

About this profile

What does Alicia U. Jacobo inspect?

Alicia U. Jacobo appears on 4 documents on file covering 4 sites, mostly in Minnesota.

What do they cite most often?

21 CFR 803.17 (what are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), followed by 21 CFR 820.198 and ISO 13485:2016 Clause 4.1.1.

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 Alicia U. Jacobo is dated Mar 12, 2026.