Form 483

TTY Biopharm Company Limited Lioudu Factory Form 483, 2022-08-30

FDA issued a Form 483 to TTY Biopharm Company Limited Lioudu Factory on 2022-08-30 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

TTY Biopharm Company Limited Lioudu Factory · Keelung City, Taiwan · Issued August 30, 2022

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

30 Aug 2022
21 CFR 211.160(a)

Deviations from laboratory control requirements

Cited by Kham Phommachanh, Rita K Kabaso

30 Aug 2022
21 CFR 211.170(b)

Reserve samples identified, representative, stored

Cited by Kham Phommachanh, Rita K Kabaso

30 Aug 2022
21 CFR 211.25(a)

Training--operations, GMPs, written procedures

Cited by Kham Phommachanh, Rita K Kabaso

30 Aug 2022
21 CFR 211.52

Washing and toilet facilities are deficient

Cited by Kham Phommachanh, Rita K Kabaso

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.170(b)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.52Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 4 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