Form 483

Precision Optics Corporation, Inc. Form 483, 2023-03-31

FDA issued a Form 483 to Precision Optics Corporation, Inc. on 2023-03-31 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Precision Optics Corporation, Inc. · Gardner, United States · Issued March 31, 2023

Overview

  • 6 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.

31 Mar 2023
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sara M Onyango

31 Mar 2023
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sara M Onyango

31 Mar 2023
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Sara M Onyango

31 Mar 2023
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Sara M Onyango

31 Mar 2023
21 CFR 820.90(b)(2)

Product rework procedures, Lack of or inadequate procedures

Cited by Sara M Onyango

Inspected site

POPrecision Optics Corporation, Inc.Gardner, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.90(b)(2)Cited across public-safe Form 483 observations2x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 6 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