Airgas USA, LLC
Form 483 issued January 12, 2024 · Salem, New Hampshire
- Inspection
- Jan 8 – Jan 12, 2024
- Investigator
- Lori M. Newman
- Observations
- 1
- Pages
- 2
- FEI number
- 1216783
In short: On January 12, 2024, FDA issued a Form 483 with 1 observation to Airgas USA, LLC in Salem, New Hampshire (FEI 1216783) after an inspection that ran Jan 8 – Jan 12, 2024. The investigator was Lori M. Newman. Most observations concern facilities & equipment; the most-cited regulation is 21 CFR 211.68 (automatic, mechanical, and electronic equipment).
At a glance
1 of 1 observations on this 483 concern facilities & equipment.
Most cited: 21 CFR 211.68(b) (1×)
What FDA observed
Preview: the opening words of each observation- 01
Appropriate controls are not exercised over computers or related systems to assure that changes in taster…
This inspection in context
Lori M. Newman
18 documents · 2021–2026
Cites 211.192 (production record review) more than any other section. Most of their documents are for sites in Massachusetts.
The firmAirgas USA, LLC history
The site's inspection history, in date order.
Similar 483sOther sites cited under 211.68(b)
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Airgas USA, LLC?
FDA listed 1 observation on this Form 483, mostly about facilities & equipment. The most-cited regulation is 21 CFR 211.68 (automatic, mechanical, and electronic equipment). The opening words of each observation are shown on this page.
Who inspected Airgas USA, LLC?
Lori M. Newman is named on this Form 483, for the inspection of Jan 8 – Jan 12, 2024. Each investigator has a profile showing what they cite most.
When was Airgas USA, LLC inspected by FDA?
The inspection ran Jan 8 – Jan 12, 2024, and the Form 483 is dated January 12, 2024.
How do I get the full Form 483 for Airgas USA, LLC?
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.