Form 483

Midlab Incorporated Form 483, 2022-08-05

FDA issued a Form 483 to Midlab Incorporated on 2022-08-05 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

Midlab Incorporated · Athens, United States · Issued August 5, 2022

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

5 Aug 2022
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Clinton J Lott

5 Aug 2022
21 CFR 211.115(a)

Reprocessing procedures not written or followed

Cited by Clinton J Lott

5 Aug 2022
21 CFR 211.165(b)

Microbiological testing

Cited by Clinton J Lott

5 Aug 2022
21 CFR 211.166(a)

Lack of written stability program

Cited by Clinton J Lott

5 Aug 2022
21 CFR 211.22(a)

Approve or reject components, products

Cited by Clinton J Lott

Inspected site

MIMidlab IncorporatedAthens, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.115(a)Cited across public-safe Form 483 observations1x
21 CFR 211.165(b)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.84(d)(1)Cited across public-safe Form 483 observations1x

Source document

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PDF available

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