← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #9 OF 1,000 MOST-CITED

Procedures not in writing, fully followed

FDA cited this observation 1,277 times across 1,086 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
Drugs1,277
BY FISCAL YEAR
FY202687
FY2025219
FY2024170
FY2023114
FY2022123
FY202168
FY202076
FY2019164
FY2018166
FY201790

What this observation is associated with

Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 3.6× the rate of the average FDA-cited firm (30.2% vs 8.3%), across 1,086 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.

CHECKING ACCESS

Checking your Professional access…

How FDA worded it — real examples

The responsibilities and procedures applicable to the quality control unit are not in writing and fully followed.

I 3 PHARMACEUTICALS, LLC · Warminster, Pennsylvania · Drugs · 2026-05-22

The responsibilities and procedures applicable to the quality control unit are not in writing and fully followed.

Apnar Pharma LLP · East Windsor, New Jersey · Drugs · 2026-05-22

The responsibilities and procedures applicable to the quality control unit are not fully followed.

Viatris Pharmaceuticals LLC · Vega Baja, Puerto Rico · Drugs · 2026-05-18

The responsibilities and procedures applicable to the quality control unit are not fully followed.

Unither Manufacturing LLC. · Rochester, New York · Drugs · 2026-05-15

The responsibilities and procedures applicable to the quality control unit are not in writing and fully followed.

Microchem Laboratory · Richardson, Texas · Drugs · 2026-04-30

The responsibilities and procedures applicable to the quality control unit are not in writing and fully followed.

Eco Lips, Inc. · Cedar Rapids, Iowa · Drugs · 2026-04-29

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 systemPharma 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.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →