Form 483

Hanlim Pharm Co. Ltd. Form 483, 2014-04-18

FDA issued a Form 483 to Hanlim Pharm Co. Ltd. on 2014-04-18 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Hanlim Pharm Co. Ltd. · Yongin, Korea (the Republic of) · Issued April 18, 2014

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

18 Apr 2014
21 CFR 211.25(a)

GMP Training Frequency

Cited by Zachery L Miller

18 Apr 2014
21 CFR 211.42(c)(10)

Aseptic Processing Area

Cited by Zachery L Miller

18 Apr 2014
21 CFR 211.67(c)

Cleaning/maintenance records not kept

Cited by Zachery L Miller

18 Apr 2014
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Zachery L Miller

18 Apr 2014
21 CFR 211.186(b)(3)

Component Name and Code

Cited by Zachery L Miller

Inspected site

HPHanlim Pharm Co. Ltd.Yongin, Korea (the Republic of)

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.186(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)Cited across public-safe Form 483 observations1x
21 CFR 211.67(c)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 observations

Every observation in full, 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