← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #615 OF 1,000 MOST-CITED

Quality policy and objectives

FDA cited this observation 36 times across 36 firms in recent inspections. Below: how it breaks down by program area and fiscal year, and real examples of how FDA worded it on Form FDA 483.

BY PROGRAM AREA
Devices36
BY FISCAL YEAR
FY20253
FY20243
FY20226
FY20213
FY20203
FY20197
FY20183
FY20175
FY20163

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 2.9× the rate of the average FDA-cited firm (22.2% vs 7.7%), across 36 FEI-matched firms.

This is an association, not causation, and reflects co-occurrence in FDA's records — not a claim that the observation caused or preceded the action.

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How FDA worded it — real examples

The quality policy was/were not established by management with executive responsibility.

VirtuSense Technologies, Inc. · Peoria, Illinois · Devices · 2025-09-18

The quality policy and quality objectives was/were not established by management with executive responsibility.

Trident Manufacturing, Inc. · Pingree Grove, Illinois · Devices · 2025-08-28

The quality policy was/were not established by management with executive responsibility.

Thera Test Laboratories, Inc. · Lombard, Illinois · Devices · 2025-04-21

The quality policy and quality objectives was/were not established by management with executive responsibility.

Dental Health Associates Of Madison, Ltd · Fitchburg, Wisconsin · Devices · 2024-09-03

The quality objectives was/were not established by management with executive responsibility.

Cumberland Biotherapeutics LLC · Sewanee, Tennessee · Devices · 2024-06-27

The quality policy and quality objectives was/were not established by management with executive responsibility.

Dry Eye Innovations LLC · Franklin, Tennessee · Devices · 2024-04-10

Related SPEQ references

Where to read the requirements behind this observation area on SPEQ. These are SPEQ's topic and audience pages — not an FDA classification of the citation.

Medical devices

Examples are a representative sample of FDA's published inspection observations. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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