Delta Pharma, Inc.
Form 483 issued November 21, 2025 · Ripley, Mississippi
- Inspection
- Nov 10 – Nov 21, 2025
- Investigator
- Jared P. Stevens
- Observations
- 2
- Pages
- 3
- FEI number
- 3004034796
In short: On November 21, 2025, FDA issued a Form 483 with 2 observations to Delta Pharma, Inc. in Ripley, Mississippi (FEI 3004034796) after an inspection that ran Nov 10 – Nov 21, 2025. The investigator was Jared P. Stevens. Most observations concern packaging & labeling and materials; the most-cited regulation is 21 CFR 211.87 (retesting of approved components, drug product containers, and closures).
At a glance
Packaging & labeling and materials account for 2 of 2 observations.
Most cited: 21 CFR 211.87 (1×)
What FDA observed
Preview: the opening words of each observationDashed: section inferred by FDA Intel and checked against the regulation text
- 01
Observation 1: scanned text, readable in the full document.
- 02
Approved components are not retested or reexamined as appropriate for identity, strength, quality and purity after…
This inspection in context
Jared P. Stevens
15 documents · 2017–2025
Cites FDCA 501(a)(2)(A) (insanitary conditions) more than any other section. Most of their documents are for sites in South Carolina.
The firmDelta Pharma, Inc. history
All 9 documents on file for this site, in date order, with what was cited at each inspection.
Similar 483sOther sites cited under 211.87
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Delta Pharma, Inc.?
FDA listed 2 observations on this Form 483, mostly about packaging & labeling and materials. The most-cited regulation is 21 CFR 211.87 (retesting of approved components, drug product containers, and closures). The opening words of each observation are shown on this page.
Who inspected Delta Pharma, Inc.?
Jared P. Stevens is named on this Form 483, for the inspection of Nov 10 – Nov 21, 2025. Each investigator has a profile showing what they cite most.
When was Delta Pharma, Inc. inspected by FDA?
The inspection ran Nov 10 – Nov 21, 2025, and the Form 483 is dated November 21, 2025.
How do I get the full Form 483 for Delta Pharma, Inc.?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.