Form 483

Allure Labs, LLC Form 483, 2017-10-25

FDA issued a Form 483 to Allure Labs, LLC on 2017-10-25 with 7 public-safe observations.

483· Form 483 issuedHuman Drugs7 observations

Allure Labs, LLC · Hayward, United States · Issued October 25, 2017

Overview

  • 7 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.

25 Oct 2017
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Kristin M Abaonza

25 Oct 2017
21 CFR 211.142

Written warehousing procedures established/followed

Cited by Kristin M Abaonza

25 Oct 2017
21 CFR 211.170(b)

Annual visual exams of drug products

Cited by Kristin M Abaonza

25 Oct 2017
21 CFR 211.170(b)

Reserve samples identified, representative, stored

Cited by Kristin M Abaonza

25 Oct 2017
21 CFR 211.180(e)(1)

Review of representative number of batches

Cited by Kristin M Abaonza

Inspected site

ALAllure Labs, LLCHayward, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.170(b)Cited across public-safe Form 483 observations2x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.142Cited across public-safe Form 483 observations1x
21 CFR 211.180(e)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.80(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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