Form 483

Geri-Care Pharmaceuticals Corp. Form 483, 2025-05-05

FDA issued a Form 483 to Geri-Care Pharmaceuticals Corp. on 2025-05-05 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Geri-Care Pharmaceuticals Corp. · Lakewood, United States · Issued May 5, 2025

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

5 May 2025
21 CFR 211.166(a)

Lack of written stability program

Cited by Tamil Arasu, Alisha B Patel

5 May 2025
21 CFR 211.170(b)

Annual visual exams of drug products

Cited by Tamil Arasu, Alisha B Patel

5 May 2025
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Tamil Arasu, Alisha B Patel

5 May 2025
21 CFR 211.22(a)

Contract drug products--lack of responsibility

Cited by Tamil Arasu, Alisha B Patel

5 May 2025
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Tamil Arasu, Alisha B Patel

Inspected site

GPGeri-Care Pharmaceuticals Corp.Lakewood, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.170(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited 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 5 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