← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #312 OF 1,000 MOST-CITED

Production and Process Change Procedures, lack of or Inad.

FDA cited this observation 69 times across 67 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
Devices69
BY FISCAL YEAR
FY20261
FY20256
FY20246
FY20235
FY20225
FY20214
FY20205
FY201912
FY201812
FY201713

How FDA worded it — real examples

Procedures for changes to a process and procedure have not been adequately established.

HG Medical Gmbh · Raisting · Devices · 2026-01-09

Procedures for changes to a specification have not been adequately established.

Exactech, Inc. · Gainesville, Florida · Devices · 2025-08-27

Procedures for changes to a process and procedure have not been adequately established.

Caragh Precision · Galway · Devices · 2025-07-17

Procedures for changes to a process have not been adequately established.

AMSUSA LLC · Atlanta, Georgia · Devices · 2025-05-06

Procedures for changes to a process have not been established.

Menasha Packaging Company LLC · Edison, New Jersey · Devices · 2025-02-18

Procedures for changes to a specification and process have not been adequately established.

PT. TEAM-METAL INDONESIA · Batam · Devices · 2024-12-04

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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