Form 483

Klocke of America, Inc. Form 483, 2022-03-30

FDA issued a Form 483 to Klocke of America, Inc. on 2022-03-30 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Klocke of America, Inc. · Fort Myers, United States · Issued March 30, 2022

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 3 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

30 Mar 2022
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Nicole E Knowlton, Damaris Y Hernandez, Dorothy P Kramer

30 Mar 2022
21 CFR 211.42(a)

Buildings of Suitable Size, Construction, Location

Cited by Nicole E Knowlton, Damaris Y Hernandez, Dorothy P Kramer

30 Mar 2022
21 CFR 211.67(a)

Cleaning / Sanitizing / Maintenance

Cited by Nicole E Knowlton, Damaris Y Hernandez, Dorothy P Kramer

30 Mar 2022
21 CFR 211.68(b)

Computer control of master formula records

Cited by Nicole E Knowlton, Damaris Y Hernandez, Dorothy P Kramer

Inspected site

KOKlocke of America, Inc.Fort Myers, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.42(a)Cited across public-safe Form 483 observations1x
21 CFR 211.67(a)Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)Cited across public-safe Form 483 observations1x

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 4 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