Arnold Professional Pharmacy

FDA inspection history across 2 sites, 2016 to 2022

3
Form 483s
2
Warning letters

Every document, by year

  • Form 483
  • Warning letter

2016: one Form 483; 2017: one warning letter; 2018: one Form 483; 2019: one warning letter; 2022: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2016–19Two Form 483s and two warning letters, at Arnold, Maryland and Maryland.
  2. 2016The longest 483 on file: 4 observations over 2 pages at Arnold, Maryland.
  3. 2022One Form 483, at Arnold, Maryland.

Cited most

Across all Arnold Professional Pharmacy observations on file

  • FDCA 501(a)(2)(A)
    Insanitary conditions
    3
  • 21 CFR 211.110
    Sampling and testing of in-process materials and drug products
    1
  • 21 CFR 211.165
    Testing and release for distribution
    1
  • 21 CFR 211.67
    Equipment cleaning and maintenance
    1
  • 21 CFR 211.68
    Automatic, mechanical, and electronic equipment
    1

The complete Arnold Professional Pharmacy file.

All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

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Sites

Documents

5 on file, newest first
DateDocumentPrice
2022-03-18483 Form 483$99
2019-12-21Warning letter Warning letter$99
2018-09-05483 Form 483$99
2017-04-07Warning letter Warning letter$99
2016-05-06483 Form 483$99

FEI number 3012283530 · most recent document Mar 18, 2022

About Arnold Professional Pharmacy

How many FDA Form 483s has Arnold Professional Pharmacy received?

FDA Intel has 3 Form 483s on file for Arnold Professional Pharmacy; the most recent is dated Mar 18, 2022.

When was Arnold Professional Pharmacy last inspected by FDA?

The most recent FDA inspection document on file for Arnold Professional Pharmacy is a Form 483 dated Mar 18, 2022, for the site in Arnold, Maryland.

What did FDA cite at Arnold Professional Pharmacy?

The regulations cited most in the observations on file for Arnold Professional Pharmacy are FDCA 501(a)(2)(A) (Insanitary conditions), 3 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time.

Has Arnold Professional Pharmacy received an FDA warning letter?

Yes. FDA Intel has 2 FDA warning letters on file for Arnold Professional Pharmacy; the most recent is dated Dec 21, 2019.

Arnold Professional Pharmacy FDA Inspection History & 483s · FDA Intel