← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #116 OF 1,000 MOST-CITED

Environmental control Lack of or inadequate procedures

FDA cited this observation 257 times across 229 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
Devices257
BY FISCAL YEAR
FY20264
FY202531
FY202420
FY202324
FY202215
FY20218
FY202026
FY201922
FY201841
FY201734
FY201632

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 1.9× the rate of the average FDA-cited firm (14.4% vs 7.7%), across 229 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 to control environmental conditions have not been adequately established.

J Sterling Industries, LLC · Kalamazoo, Michigan · Devices · 2026-01-08

Procedures to control environmental conditions have not been adequately established.

MEDTRONIC GRAND RAPIDS · Grand Rapids, Michigan · Devices · 2025-12-15

Procedures to control environmental conditions have not been adequately established.

3D Diagnostix Inc. · Allston, Massachusetts · Devices · 2025-11-21

Procedures to control environmental conditions have not been adequately established.

Riverside Medical Packaging Company Ltd · Derby · Devices · 2025-10-16

Procedures to control environmental conditions have not been adequately established.

rms Company · Minneapolis, Minnesota · Devices · 2025-09-12

Procedures to control environmental conditions have not been established.

Keter Canada, Inc. · Milton · Devices · 2025-09-05

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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