Form 483

Lotus Pharmaceutical Co., Ltd. Nantou Plant Form 483, 2017-09-22

FDA issued a Form 483 to Lotus Pharmaceutical Co., Ltd. Nantou Plant on 2017-09-22 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

Lotus Pharmaceutical Co., Ltd. Nantou Plant · Nantou County, Taiwan · Issued September 22, 2017

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

22 Sep 2017
21 CFR 211.160(b)(3)

Drug products - samples representative, identified properly

Cited by Jessica L Pressley

22 Sep 2017
21 CFR 211.170(b)

Annual visual exams of drug products

Cited by Jessica L Pressley

22 Sep 2017
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Jessica L Pressley

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.170(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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