Form 483

Recipharm Pharmaservices Private Limited Form 483, 2019-02-01

FDA issued a Form 483 to Recipharm Pharmaservices Private Limited on 2019-02-01 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

Recipharm Pharmaservices Private Limited · Bengaluru, India · Issued February 1, 2019

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.

1 Feb 2019
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Marcus A Ray

1 Feb 2019
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Marcus A Ray

1 Feb 2019
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Marcus A Ray

1 Feb 2019
21 CFR 211.63

Equipment Design, Size and Location

Cited by Marcus A Ray

1 Feb 2019
21 CFR 211.63

Equipment Design, Size and Location

Cited by Marcus A Ray

Inspected site

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 observations2x
21 CFR 211.113(a)Cited across public-safe Form 483 observations2x
21 CFR 211.63Cited across public-safe Form 483 observations2x

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 6 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