Delta Pharma, Inc.
Form 483 issued June 2, 2023 · Ripley, Mississippi
- Inspection
- May 22 – Jun 2, 2023
- Investigator
- Sonya M. Edmonds
- Observations
- 1
- Pages
- 2
- FEI number
- 3004034796
In short: On June 2, 2023, FDA issued a Form 483 with 1 observation to Delta Pharma, Inc. in Ripley, Mississippi (FEI 3004034796) after an inspection that ran May 22 – Jun 2, 2023. The investigator was Sonya M. Edmonds. Most observations concern facilities & equipment; the most-cited regulation is 21 CFR 211.42 (design and construction features).
At a glance
1 of 1 observations on this 483 concern facilities & equipment.
Most cited: 21 CFR 211.42(c)(10)(iv) (1×)
What FDA observed
Preview: the opening words of each observation- 01
Aseptic processing areas are deficient regarding the system…
This inspection in context
Sonya M. Edmonds
12 documents · 2016–2025
Cites 211.42 (design and construction features) more than any other section. Most of their documents are for sites in North 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 211.42(c)(10)(iv)
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Delta Pharma, Inc.?
FDA listed 1 observation on this Form 483, mostly about facilities & equipment. The most-cited regulation is 21 CFR 211.42 (design and construction features). The opening words of each observation are shown on this page.
Who inspected Delta Pharma, Inc.?
Sonya M. Edmonds is named on this Form 483, for the inspection of May 22 – Jun 2, 2023. Each investigator has a profile showing what they cite most.
When was Delta Pharma, Inc. inspected by FDA?
The inspection ran May 22 – Jun 2, 2023, and the Form 483 is dated June 2, 2023.
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.