Ackerman Nuclear, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Ackerman Nuclear, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Ackerman Nuclear, Inc." is on file.

What these totals cover: FDA records filed under the name "Ackerman Nuclear, Inc." and its spelling variant "Ackerman Nuclear".

Latest 510(k)
Nov 19, 1976

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

1 510(k) clearance on Nov 19, 1976.

K-NumberDeviceDate
K760908MINIATURE ASCENDING PAPER CHROMATO-Nov 19, 1976

Ackerman Nuclear, Inc. and the FDA: common questions

Has Ackerman Nuclear, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Ackerman Nuclear, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Ackerman Nuclear, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Ackerman Nuclear, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.