← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #521 OF 1,000 MOST-CITED

Not approved or obsolete document retrieval

FDA cited this observation 36 times across 35 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
FY20252
FY20242
FY20235
FY20222
FY20204
FY20198
FY20184
FY20179

How FDA worded it — real examples

Documents that were not approved were observed at a location where they are being used.

Donson Machine Company · Alsip, Illinois · Devices · 2025-08-18

Documents that were obsolete were observed at a location where they are being used.

MedHab, LLC · Fort Worth, Texas · Devices · 2024-11-27

Documents that were not approved were observed at a location where they are being used.

Skeletal Dynamics, Inc. · Miami, Florida · Devices · 2024-04-05

Documents that were obsolete were observed at a location where they are being used.

Taiji Medical Supplies Inc. · Lincolnton, North Carolina · Devices · 2024-03-15

Documents that were not approved and obsolete were observed at a location where they could be used.

iScreen Vision, Inc. · Cordova, Tennessee · Devices · 2023-09-28

Documents that were not approved were observed at a location where they could be used.

Robin Industries, Inc. · Millersburg, Ohio · Devices · 2023-09-26

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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