Central Admixture Pharmacy Services, Inc.

Form 483 issued September 19, 2016 · Allentown, Pennsylvania

Inspection
Aug 29 – Sep 19, 2016
Investigator
James M. Mason
Observations
2
Pages
4
FEI number
3009590582

In short: On September 19, 2016, FDA issued a Form 483 with 2 observations to Central Admixture Pharmacy Services, Inc. in Allentown, Pennsylvania (FEI 3009590582) after an inspection that ran Aug 29 – Sep 19, 2016. The investigator was James M. Mason. Most observations concern quality system and materials; the most-cited regulation is 21 CFR 211.192 (production record review).

At a glance

Quality system and materials account for 2 of 2 observations.

Quality system1
Materials1

Most cited: 21 CFR 211.192 (1×) · 211.142 (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 a failure to thoroughly review any unexplained discrepancy whether or not the batch…

  2. 02

    Procedures describing the warehousing of dmg…

The full 483

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This inspection in context

Questions about this 483

What did FDA find at Central Admixture Pharmacy Services, Inc.?

FDA listed 2 observations on this Form 483, mostly about quality system and materials. The most-cited regulation is 21 CFR 211.192 (production record review). The opening words of each observation are shown on this page.

Who inspected Central Admixture Pharmacy Services, Inc.?

James M. Mason is named on this Form 483, for the inspection of Aug 29 – Sep 19, 2016. Each investigator has a profile showing what they cite most.

When was Central Admixture Pharmacy Services, Inc. inspected by FDA?

The inspection ran Aug 29 – Sep 19, 2016, and the Form 483 is dated September 19, 2016.

How do I get the full Form 483 for Central Admixture Pharmacy Services, Inc.?

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