Form 483

Hi-Tech Pharmacal, an AKORN Company Form 483, 2008-11-04

FDA issued a Form 483 to Hi-Tech Pharmacal, an AKORN Company on 2008-11-04 with 4 public-safe observations.

483· Form 483 issued4 observations

Hi-Tech Pharmacal, an AKORN Company · Amityville, United States · Issued November 4, 2008

Overview

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

4 Nov 2008
21 CFR 211.100(b)

Procedure Deviations Recorded and Justified

Cited by Robert C Steyert

4 Nov 2008
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Robert C Steyert

4 Nov 2008
21 CFR 211.198(a)

Reporting of adverse drug experience to FDA

Cited by Robert C Steyert

4 Nov 2008
21 CFR 314.80(c)(1)(i)

Late submission of 15-day report

Cited by Robert C Steyert

Inspected site

HPHi-Tech Pharmacal, an AKORN CompanyAmityville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.198(a)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(1)(i)Cited across public-safe Form 483 observations1x

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