Form 483

Esco Medical Technologies Ltd. Form 483, 2018-02-08

FDA issued a Form 483 to Esco Medical Technologies Ltd. on 2018-02-08 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Esco Medical Technologies Ltd. · Ramuciai, Lithuania · Issued February 8, 2018

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.

8 Feb 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Charles L Larson

8 Feb 2018
21 CFR 820.40(a)

Document review, approval documentation

Cited by Charles L Larson

8 Feb 2018
21 CFR 820.40(a)

Document review, approval documentation

Cited by Charles L Larson

8 Feb 2018
21 CFR 820.50(a)(1)

Documented evaluation

Cited by Charles L Larson

8 Feb 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Charles L Larson

Inspected site

EMEsco Medical Technologies Ltd.Ramuciai, Lithuania

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.40(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 6 observations

The full inspection record, as Atlas holds it, 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