Form 483

FORDOZ PHARMA CO. Form 483, 2023-03-17

FDA issued a Form 483 to FORDOZ PHARMA CO. on 2023-03-17 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

FORDOZ PHARMA CO. · East Windsor, United States · Issued March 17, 2023

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.

17 Mar 2023
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Alice S Tsao, Pushpa S Jayasekara

17 Mar 2023
21 CFR 211.142

Written warehousing procedures established/followed

Cited by Alice S Tsao, Pushpa S Jayasekara

17 Mar 2023
21 CFR 211.42(a)

Buildings of Suitable Size, Construction, Location

Cited by Alice S Tsao, Pushpa S Jayasekara

17 Mar 2023
21 CFR 211.63

Equipment Design, Size and Location

Cited by Alice S Tsao, Pushpa S Jayasekara

Inspected site

FPFORDOZ PHARMA CO.East Windsor, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.142Cited across public-safe Form 483 observations1x
21 CFR 211.42(a)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited 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