← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #212 OF 1,000 MOST-CITED

Batch production and Batch Control Record Requirements

FDA cited this observation 138 times across 130 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
Drugs138
BY FISCAL YEAR
FY20266
FY202514
FY20249
FY20238
FY202211
FY202112
FY202013
FY201921
FY201812
FY201722
FY201610

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 5.6× the rate of the average FDA-cited firm (43.1% vs 7.7%), across 130 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

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in manufacturing and processing.

Hyland's Consumer Health Inc. · Los Angeles, California · Drugs · 2026-04-22

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in manufacturing.

Gallant Pet Inc · San Diego, California · Drugs · 2026-02-27

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in processing, packing and holding.

St Mary's Medical Park Pharmacy · Oro Valley, Arizona · Drugs · 2025-12-04

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in manufacturing, processing, packing and holding.

Actavis Laboratories FL, Inc. · Davie, Florida · Drugs · 2025-11-18

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in manufacturing and processing.

Jubilant HollisterStier General Partnership · Kirkland · Drugs · 2025-11-03

The batch production and control records are deficient in that they do not include documentation of the accomplishment of each significant step in manufacturing.

CareFusion 213, LLC · El Paso, Texas · Drugs · 2025-10-24

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.

Pharma industry

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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