DESIGN CATAPULT MANUFACTURING, INC
Form 483 issued August 19, 2025 · Fountain Valley, California
- Inspection
- Aug 14 – Aug 19, 2025
- Investigator
- Alexandria L. Capuano
- Observations
- 1
- Pages
- 3
- FEI number
- 3015414274
In short: On August 19, 2025, FDA issued a Form 483 with 1 observation to DESIGN CATAPULT MANUFACTURING, INC in Fountain Valley, California (FEI 3015414274) after an inspection that ran Aug 14 – Aug 19, 2025. The investigator was Alexandria L. Capuano. Most observations concern cAPA; the most-cited regulation is 21 CFR 820.100 (corrective and preventive action).
At a glance
1 of 1 observations on this 483 concern capa.
Most cited: 21 CFR 820.100(b) (1×)
What FDA observed
Preview: the opening words of each observation- 01
Corrective and preventive action activities and/or results have…
This inspection in context
Alexandria L. Capuano
6 documents · 2022–2026
Cites 820.198 (complaint files) more than any other section. Most of their documents are for sites in California.
The firmDESIGN CATAPULT MANUFACTURING, INC history
The site's inspection history, in date order.
Similar 483sOther sites cited under 820.100(b)
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at DESIGN CATAPULT MANUFACTURING, INC?
FDA listed 1 observation on this Form 483, mostly about cAPA. The most-cited regulation is 21 CFR 820.100 (corrective and preventive action). The opening words of each observation are shown on this page.
Who inspected DESIGN CATAPULT MANUFACTURING, INC?
Alexandria L. Capuano is named on this Form 483, for the inspection of Aug 14 – Aug 19, 2025. Each investigator has a profile showing what they cite most.
When was DESIGN CATAPULT MANUFACTURING, INC inspected by FDA?
The inspection ran Aug 14 – Aug 19, 2025, and the Form 483 is dated August 19, 2025.
How do I get the full Form 483 for DESIGN CATAPULT MANUFACTURING, INC?
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