← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #285 OF 1,000 MOST-CITED

Statistical techniques - Lack of or inadequate procedures

FDA cited this observation 77 times across 76 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
Devices77
BY FISCAL YEAR
FY20261
FY20258
FY20247
FY202310
FY20227
FY20215
FY20208
FY201911
FY20189
FY201711

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 0.9× the rate of the average FDA-cited firm (7.9% vs 8.3%), across 76 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

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been adequately established.

Turbett Surgical, Inc. · Henrietta, New York · Devices · 2025-11-06

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been established.

Keystone Industries · Gibbstown, New Jersey · Devices · 2025-09-30

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been established.

MACLEAN-FOGG · Menomonee Falls, Wisconsin · Devices · 2025-05-22

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been adequately established.

R-Med Inc · Oregon, Ohio · Devices · 2025-04-23

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been established.

Boston Scientific Corporation · Saint Paul, Minnesota · Devices · 2025-04-07

Procedures for identifying valid statistical techniques required for establishing, controlling, and verifying the acceptability of process capability and product characteristics have not been adequately established.

KANEKA MEDICAL VIETNAM Co.,Ltd. · Thuan An · Devices · 2025-02-13

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.

Pharmaceutical quality systemMedical 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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