Form 483

Lyne Laboratories, Inc. Form 483, 2016-08-17

FDA issued a Form 483 to Lyne Laboratories, Inc. on 2016-08-17 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Lyne Laboratories, Inc. · Brockton, United States · Issued August 17, 2016

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

17 Aug 2016
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Robert J Martin

17 Aug 2016
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Robert J Martin

17 Aug 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Robert J Martin

17 Aug 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Robert J Martin

Inspected site

LLLyne Laboratories, Inc.Brockton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations2x
21 CFR 211.192Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 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