Form 483

GRAM Laboratories, Inc. Form 483, 2025-04-08

FDA issued a Form 483 to GRAM Laboratories, Inc. on 2025-04-08 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

GRAM Laboratories, Inc. · Irvine, United States · Issued April 8, 2025

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

8 Apr 2025
21 CFR 211.192

Written record of investigation incomplete

Cited by Wenzheng Zhang

8 Apr 2025
21 CFR 211.25(a)

GMP Training Frequency

Cited by Wenzheng Zhang

8 Apr 2025
21 CFR 211.63

Equipment Design, Size and Location

Cited by Wenzheng Zhang

Inspected site

GLGRAM Laboratories, Inc.Irvine, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 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