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Global Packaging Systems, Inc

FDA establishment 3003306559, Fort Worth, Texas, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.

  • Inspections: 5
  • Official action indicated: 0
  • Last inspection ended: Apr 9, 2026
  • Warning letters: 0

Inspections by Fiscal Year

FY2018 to FY2027 to date; 0 classified OAI

Most Cited at This Site

Inspections citing each reference

Inspections

5 inspections, newest first
EndedProduct and areaCitationsClassification
Apr 9, 2026Drugs · Drug Quality Assurance
4 cited references
  • 21 CFR 211.22(d). Procedures not in writing, fully followed The responsibilities and procedures applicable to the quality control unit are not in writing and fully followed.
  • 21 CFR 211.150. Written distribution procedure Written distribution procedures are not established.
  • 21 CFR 211.142(b). Storage under appropriate conditions Drug products are not stored under appropriate conditions of temperature so that their identity, strength, quality, and purity are not affected.
  • 21 CFR 211.68(a). Calibration/Inspection/Checking not done Routine calibration of electronic equipment is not performed according to a written program designed to assure proper performance.
Voluntary Action Indicated (VAI)
Dec 29, 2022Devices · Compliance: DevicesDevices · Postmarket Assurance: DevicesNone postedNo Action Indicated (NAI)
Jan 15, 2013Drugs · Drug Quality Assurance
2 cited references
  • 21 CFR 211.130(e). Packaging line inspection before use Inspection of the packaging and labeling facilities immediately before use is not done to assure that all drug products have been removed from previous operations.
  • 21 CFR 211.182. Written records kept in individual logs Written records of major equipment maintenance are not included in individual equipment logs.
Voluntary Action Indicated (VAI)
Dec 7, 2011Drugs · Drug Quality AssuranceNone postedNo Action Indicated (NAI)
Jan 13, 2010Drugs · Drug Quality AssuranceNone postedVoluntary Action Indicated (VAI)

Identifiers

FEI number
3003306559
FDA firm profile
Data Dashboard

An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard and warning letters

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.