Form 483

East Marietta Drug Company Form 483, 2019-08-23

FDA issued a Form 483 to East Marietta Drug Company on 2019-08-23 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

East Marietta Drug Company · Marietta, United States · Issued August 23, 2019

Overview

  • 3 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

23 Aug 2019
FDCA 501(a)(2)(A)

Highly potent drugs, prevention of cross-contamination

Cited by Gideon N Esuzor, Johnetta F Walters

23 Aug 2019
FDCA 501(a)(2)(A)

Non-microbial contamination, production area

Cited by Gideon N Esuzor, Johnetta F Walters

23 Aug 2019
FDCA 501(a)(2)(A)

Personnel habits, contamination

Cited by Gideon N Esuzor, Johnetta F Walters

Inspected site

EMEast Marietta Drug CompanyMarietta, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
FDCA 501(a)(2)(A)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 3 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