Centrix, Inc.

Form 483 issued January 31, 2017 · Shelton, Connecticut

Inspection
Jan 5 – Jan 31, 2017
Investigator
Dien N. Nguyen
Observations
2
Pages
5
FEI number
1261412

In short: On January 31, 2017, FDA issued a Form 483 with 2 observations to Centrix, Inc. in Shelton, Connecticut (FEI 1261412) after an inspection that ran Jan 5 – Jan 31, 2017. The investigator was Dien N. Nguyen. Most observations concern laboratory controls and materials; the most-cited regulation is 21 CFR 211.166 (stability testing).

At a glance

Laboratory controls and materials account for 2 of 2 observations.

Laboratory controls1
Materials1

Most cited: 21 CFR 211.166 (1×) · 211.82 (1×)

What FDA observed

Preview: the opening words of each observation

Dashed: section inferred by FDA Intel and checked against the regulation text

  1. 01

    There is no written testing program designed to assess the stability…

  2. 02

    Each container or grouping of containers of components is not examined before acceptance for appropriate…

The full 483

Plus the full detail behind each one, exactly as FDA wrote it.

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This inspection in context

Questions about this 483

What did FDA find at Centrix, Inc.?

FDA listed 2 observations on this Form 483, mostly about laboratory controls and materials. The most-cited regulation is 21 CFR 211.166 (stability testing). The opening words of each observation are shown on this page.

Who inspected Centrix, Inc.?

Dien N. Nguyen is named on this Form 483, for the inspection of Jan 5 – Jan 31, 2017. Each investigator has a profile showing what they cite most.

When was Centrix, Inc. inspected by FDA?

The inspection ran Jan 5 – Jan 31, 2017, and the Form 483 is dated January 31, 2017.

How do I get the full Form 483 for Centrix, Inc.?

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