← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #582 OF 1,000 MOST-CITED

Design plans - Lack of or inadequate

FDA cited this observation 40 times across 38 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
Devices40
BY FISCAL YEAR
FY20257
FY20246
FY20236
FY20223
FY20212
FY20203
FY20194
FY20184
FY20165

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 0.7× the rate of the average FDA-cited firm (5.3% vs 7.7%), across 38 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

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been established.

In2Bones, SAS · Ecully · Devices · 2025-09-04

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been adequately established.

DGI Group LLC · Howell, New Jersey · Devices · 2025-08-19

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been established.

Blue Elephant Inc · Southlake, Texas · Devices · 2025-05-16

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been established.

Auxilium Medical Inc. · Charleston, South Carolina · Devices · 2025-03-26

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been established.

Vayuclear Inc · Charleston, South Carolina · Devices · 2025-03-14

Design plans that describe or reference the design and development activities and define responsibility for implementation have not been adequately established.

Stabiliz Orthopaedics · Exton, Pennsylvania · Devices · 2024-12-09

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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