Form 483

Ernest Jackson & Co., Ltd. Form 483, 2019-08-08

FDA issued a Form 483 to Ernest Jackson & Co., Ltd. on 2019-08-08 with 12 public-safe observations.

483· Form 483 issuedHuman Drugs12 observations

Ernest Jackson & Co., Ltd. · Crediton, United Kingdom · Issued August 8, 2019

Overview

  • 12 public-safe observations are available for this inspection.
  • 6 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

8 Aug 2019
21 CFR 211.165(b)

Microbiological testing

Cited by Emilie Kahn

8 Aug 2019
21 CFR 211.170(b)

Investigation of reserve sample deterioration

Cited by Emilie Kahn

8 Aug 2019
21 CFR 211.46(b)

Equipment for Environmental Control

Cited by Emilie Kahn

8 Aug 2019
21 CFR 211.63

Equipment Design, Size and Location

Cited by Emilie Kahn

8 Aug 2019
21 CFR 211.67(b)

Written procedures not established/followed

Cited by Emilie Kahn

Inspected site

EJErnest Jackson & Co., Ltd.Crediton, United Kingdom

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.165(b)Cited across public-safe Form 483 observations2x
21 CFR 211.170(b)Cited across public-safe Form 483 observations2x
21 CFR 211.46(b)Cited across public-safe Form 483 observations2x
21 CFR 211.63Cited across public-safe Form 483 observations2x
21 CFR 211.67(b)Cited across public-safe Form 483 observations2x
21 CFR 211.80(a)Cited across public-safe Form 483 observations2x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 12 observations

The source PDF, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere