Form 483

Micro Current Technology, Inc. Form 483, 2019-01-28

FDA issued a Form 483 to Micro Current Technology, Inc. on 2019-01-28 with 9 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health9 observations

Micro Current Technology, Inc. · Seattle, United States · Issued January 28, 2019

Overview

  • 9 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.

28 Jan 2019
21 CFR 820.250(b)

Sampling plans

Cited by Stephen R Souza

28 Jan 2019
21 CFR 820.30(g)

Design validation - software validation not performed

Cited by Stephen R Souza

28 Jan 2019
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Stephen R Souza

28 Jan 2019
21 CFR 820.250(b)

Sampling plans

Cited by Stephen R Souza

28 Jan 2019
21 CFR 820.250(b)

Sampling plans

Cited by Stephen R Souza

Inspected site

MCMicro Current Technology, Inc.Seattle, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.250(b)Cited across public-safe Form 483 observations3x
21 CFR 820.30(g)Cited across public-safe Form 483 observations3x
21 CFR 820.30(i)Cited across public-safe Form 483 observations3x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 9 observations

The source PDF and 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